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Evidera

32 💼 Evidera Jobs / Employment

Research Associate I - Modeling and Simulation

newabout 15 hours ago
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Research Associate I - Modeling and SimulationOur multidisciplinary Modeling and Simulation experts design and implement health economic models that describe complex medical processes to understand and evaluate the implications of clinical trials; demonstrate the value of interventions beyond efficacy, and assess benefits, risks, and the economic consequences associated with healthcare interventions. If you have a passion for health economic modeling to conduct cost-effectiveness analyses of healthcare interventions and have experience conceptualizing and implementing simulation models (e.g., discrete event simulation) and other decision-analytic models (e.g., decision trees, Markov, individual state-transition, survival partition), a position in Modeling and Simulation at Evidera is waiting for you!Position OverviewAssist with implementing simulation models (e.g., discrete event simulation) and other decision-analytic models (e.g., Markov, individual state-transition, survival partition) to assess the cost-effectiveness of healthcare interventions. Assist with scientific and financial project management, and monitoring progress for projects when assigned.Essential Duties and Responsibilities: (other duties may be assigned)Assist with implementing one or more of the following (under supervision):Development of health economic models to conduct cost-effectiveness and budget impact analyses of healthcare interventions.Program models using Microsoft Excel with Visual Basic for Applications (VBA).Conduct analyses and presentation of results.Conduct literature reviews with emphasis on extracting data pertinent to health economic evaluations and cost-effectiveness analyses.Conduct basic statistical analyses (e.g., descriptive statistics and regression analysis).Assist with drafting sections of project deliverables (e.g., user guides, model specifications and technical reports).Participate in client meetings and draft meeting minutes.Assist with tracking budget and expenses and monitoring timelines and deliverables for projects when assigned.Support other "non-billable" activities as needed (e.g., assist with developing sections of proposals).Travel may be required.Education and ExperienceMaster’s degree in Health Economics, Mathematics, or Epidemiology with more than one year of relevant work experience. Master’s or Bachelor’s degrees in other fields will be considered (e.g. Operations Research or Industrial Engineering) with relevant experience of programming decision analytic models (e.g. decision trees, Markov, survival partition) in Microsoft Excel with VBA.What you bring to EvideraBasic understanding of research methods. Practical knowledge of research project implementation.Experience working with modeling/simulation software, in particular Microsoft Excel using VBA.Excellent computer skills, including Microsoft Word and PowerPoint.Strong quantitative skills, with solid understanding of basic statistics.Energy, a great work attitude and fit well with our team. Strong organization skills.Language SkillsCompetent in written and spoken English.Computer SkillsRequired: Excel and VBA expertise, Microsoft Word, Microsoft PowerPointDesired: Experience using other simulation and/or decision-analysis software (e.g., Arena, TreeAge). Company SummaryEvidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology.Why Choose Evidera?Evidera offers a competitive salary and benefits package, with clear opportunities for growth and career progression. You will have the opportunity to work on multiple projects with some of the industry’s leading researchers. Our offices boast a fun and collaborative working environment, frequent social events and a robust support system. We are committed to providing training and professional development, with ample opportunity to advance, for all our staff.Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race,color, religion, sex, national origin, age, genetics, sexual orientation, gender preference disability, or status as a qualified individual with a disability or protected veteran.

Research Associate I - Modeling and Simulation

newabout 16 hours ago
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Research Associate I - Modeling and SimulationOur multidisciplinary Modeling and Simulation experts design and implement health economic models that describe complex medical processes to understand and evaluate the implications of clinical trials; demonstrate the value of interventions beyond efficacy, and assess benefits, risks, and the economic consequences associated with healthcare interventions.If you have a passion for health economic modeling to conduct cost-effectiveness analyses of hea

Senior Manager, Real World Evidence - Data Analytics

newabout 17 hours ago
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Senior Manager, Real World Evidence, Data Analytics-US East Coast, Bethesda preferredThis is an exciting opportunity to join our successful research team and to help define and drive solutions for clients and patients.We are specifically recruiting someone for our Data Analytics team within Real-World Evidence to provide strategic oversight and project management support for a multi-million dollar program of research for one or more key accounts.This is a dynamic role involving regular contact

Senior Manager, Real World Evidence - Data Analytics

newabout 18 hours ago
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Senior Manager, Real World Evidence, Data Analytics–US East Coast, Bethesda preferredThis is an exciting opportunity to join our successful research team and to help define and drive solutions for clients and patients. We are specifically recruiting someone for our Data Analytics team within Real-World Evidence to provide strategic oversight and project management support for a multi-million dollar program of research for one or more key accounts.This is a dynamic role involving regular contact with several key internal and sponsor stakeholders. The Team Evidera has been providing epidemiology, data analytics, and outcomes research services to clients in the biopharmaceutical industry for over 19 years. The Real-World Evidence team supports pharmaceutical, biotechnology and medical device companies in the design and conduct of real-world observational studies throughout the product lifecycle, from early pre-launch planning to launch and post-marketing management. Our focus is on helping our clients identify evidence gaps and rapidly build epidemiologic and economic evidence to demonstrate the effectiveness, safety and value of their products. For this role, the focus is on observational epidemiologic studies both retrospective and prospective in nature, targeted literature reviews, and risk management plans. Data collected in these studies is then used to address key research questions such as:Burden of disease and identification of unmet needsTreatment patterns, drug utilization, adherence Resource utilizationThe identification and impact of risk factors on disease outcomes Comparative effectivenessSafety outcomes We use epidemiologic methods to build knowledge of the relationships between patient, drug, clinical and disease factors that significantly aids our clients and the patients they serve in understanding health conditions and navigating potential drug-event causal relationships as well as in building stronger evidence-based value messages. Role and ResponsibilitiesThe Senior Project Manager reports to the Executive Director. He/she supports the Executive Sponsor in the strategic oversight and management of a diverse portfolio of work for one or more key accounts. This involves the collection, tracking, and processing of data to inform decision making, managing the day-to-day communication between the sponsor and internal stakeholders, ensuring project budgets and timelines are being managed appropriately, facilitation of internal and sponsor meetings to discuss strategic planning, business development, pipeline updates, share lessons learned, and enhance client service. In particular, the Senior Project Manager will:Be responsible for the overall coordination and management of administrative aspects of individual studies from receipt of lead through project set-up and delivery to the sponsor, including but not limited to financial and legal aspects of project management. Be responsible for financial stewardship and dashboard reporting of the account, per sponsor requirements. Work to ensure that all project deliverables meet the customer time/quality/cost expectations.Work with senior management and functional area leads to identify and evaluate fundamental issues on the project and ensure solutions are implemented. Able to escalate and communicate risks and concerns, as well as develop mitigation plans specific to project needsOversee and manage diverse real-world evidence projects for multiple stakeholders within a key account; perform traditional project management activities such as ensuring all project deliverables, timelines, and budgets are closely monitored, as well as oversee Quality Control processes, ensure appropriate documentation of quality validation steps, oversee and manage third-party vendors, and keep relevant internal and sponsor stakeholders informed/consulted as appropriate.Contribute to the design and refinement of accounts-specific tools and processes as needed to meet or exceed client expectations with regards to account management. Support client communication, both providing key messaging to internal team members, but also disseminating study team communications to clients and external stakeholdersWork across functional groups and departments to ensure successful delivery of studies, including but not limited to data analytics programmers and research scientists. Engage internal teams in discussions to share lessons learned, share ideas for improvement, and discuss strategic approach to Real-World Evidence positioning and business development. Support new sales opportunities including, but not limited to, budget development, proposal content development, and ‘win’ strategiesProvide support for the Data Analytics Sr Leadership Team in defining and meeting specific business targetsIdentify opportunities to expand the account and enhance client service; propose solutions and recommendations both internally and to the sponsor directly. Work on site at client offices 40-60% of work week; regularly meet face-to-face with key client contacts to discuss status of ongoing studies, pipeline, and administrative topics. Qualifications and Experience Bachelor’s degree or licensed certified health care training or equivalent combination of education and experience that provides the individual with the required knowledge, skills and abilities.Project management certification (e.g. PMP, PgMP, CAPM) or demonstration of project management skills including scope, budgeting, forecasting, timelines, resource management, and use of project management systems (e.g. MS Project). Demonstrable experience managing across a range of cross-functional, global, external stakeholders.A demonstrated track record of project managing a variety of studies within ideally either a CRO or consulting firmA deep understanding of the Life Science industry In depth understanding of observational projects and project portfolio managementStrong written and verbal communication Proven ability to multitask and problem solve Excellent client facing skills Valid Passport, where appropriate.The position is permanent, full time and optimally based in Bethesda; 40-60% working on-site at sponsor’s office. Company SummaryEvidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science, operational excellence, and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology. Why ChooseEvidera?Evidera offers a competitive salary and benefits package. Our Bethesda office is conveniently located a few blocks from the Bethesda metro, local shops, and restaurants. This office also offers complimentary coffee & tea, breakfast on Fridays, frequent social events, and a spacious, quiet work environment. We are committed to providing training and professional development, with ample opportunity to advance for all our staff. The Real-World Evidence team constitutes a vibrant and dynamic group of individuals who specialize in scientific methods and research operations. Our mission is to be the global leader in generating and communicating evidence of product value to inform healthcare decision making.Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race,color, religion, sex, national origin, age, genetics, sexual orientation, gender preference disability, or status as a qualified individual with a disability or protected veteran.

Senior Systematic Reviewer (Research Associate III) Meta Research (Waltham MA or London UK)

newabout 18 hours ago
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Senior Systematic Reviewer (Research Associate III) – Meta Research (Waltham MA or London UK)**We are looking to fill this role in our Waltham, MA or London, UK officesThe TeamDo you have what it takes to conduct high-quality systematic literature reviews (SLRs)? Just about anyone seeking published articles to answer research questions can type terms into a database and then hope to make sense of the information retrieved. But when done without the right knowledge, skills, and experience, such an exercise risks answers that are biased, confusing, incomplete, or wholly incorrect. Poorly designed search algorithms, unworkable PICOS criteria and failure to follow PRISMA study-reporting guidelines are just a few of many things that often go wrong with such attempts at literature reviewing. This helps explain what makes Meta Research different. Our SLRs and related meta-analyses reflect broad clinical knowledge and expertise in finding and assessing complex information. This means our clients and Evidera colleagues can rely on us to discover, synthesize, and contextualize the data that really matter and thereby provide them with insights they could not have obtained by themselves. Here are just some of the things our SLRs help our clients and colleagues to do:Understand new indications in context of specific product strategyInform planning for primary research, such as choice of patient-reported outcome instruments and comparatorsEstimate clinical comparisons of products versus competitorsCapitalize on existing research while assessing evidence gapsProvide information for value development planningDetermine which databases have proved useful in target indicationsDerive model inputsCreate burden-of-illness assessments for submission to payersPublish burden assessments for disseminationPopulate dossiersPopulate regulatory documents such as Risk Management Plans.The RoleWe are looking for a Research Associate III (Senior Systematic Reviewer) for our Meta Research team in our Waltham, MA or London, UK offices. This role will independently direct key aspects of systematic literature review (SLR) research projects with guidance from senior staff, as well as manage multiple projects with tasks varying to degree by project.Responsibilities:Define and refine research questions as they pertain to the SLR objectivesDesign of literature searches/algorithms to be implemented in scientific literature databases (i.e., PubMed, EMBASE, Cochrane Library, etc.) and grey literature sources (conference proceedings, regulatory agencies). Develop inclusion/exclusion criteria within the PICOS framework to be implemented during screening processOversee the screening of abstracts and full-text articles against defined inclusion/exclusion criteria to assess their suitability for inclusion in the reviewReview the PRISMA diagram depicting the study attritionValidate data abstraction and extractionFinalize the analyzable datasetDraft tables and figures for analysis resultsSynthesize the evidence base by through drafting and editing sections of project deliverables (e.g. reports, protocols, statistical analysis plans) and dissemination actives, abstract and manuscript preparationDelegate tasks to junior staff and review their work as appropriateDevelop a project plan and monitor project progress, including timeline and budgetDraft project proposals, including scoping the body of evidence and preparing project budgets)Co-lead (or lead) client communications, both via email, phone, and in-person; responsible for day-to-day communicationsParticipate in non-literature based research and consulting activities within other departments (e.g., modeling and simulation, real-world evidence). Participate in staff recruitment and training effortsServe as a line manager (depending on skills/experience)Qualifications and ExperiencePhD in health sciences, economics, biology, natural sciences or a related field with some related experience; MSc. with significant related experience, or Bachelors with extensive related experienceProven experience in systematic literature review methods in health economics and/or health services research; experience in network meta-analysis would be an advantage, but is not essentialCommercial experience in a similar environment is highly desirable, but not essentialDeep understanding of research principles and demonstrated practical research implementationCompany SummaryEvidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology.Why Choose Evidera?Evidera offers a competitive salary and benefits package. We are committed to providing training and professional development, with ample opportunity to advance for all of our staff. Both our Waltham and London offices are conveniently located close to transport links, local shops, and restaurants. In addition, both offices offer complimentary coffee & tea, breakfast on Fridays, frequent social events, and a spacious, quiet work environment. Our mission is to be the global leader in generating and communicating evidence of product value to inform healthcare decision making.How to ApplyTo apply, please complete your online profile by attaching your CV and covering letter addressing your suitability for the role. All applications are reviewed, and qualified candidates will be contacted. Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, sexual orientation, gender preference disability, or status as a qualified individual with a disability or protected veteran.

Senior systematic reviewer research associate iii meta research waltham ma or london uk

newabout 19 hours ago
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Senior Systematic Reviewer (Research Associate III) – Meta Research (Waltham MA or London UK) We are looking to fill this role in our Waltham, MA or London

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Senior Global Recruiter Human Resources (Waltham, MA or

newabout 20 hours ago
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Senior Global Recruiter – Human Resources Position Overview: Reporting to the Executive Director of Global Recruitment, serves as a senior point of contact within assigned practice areas of Evidera’s talent acquisition program. The incumbent works across the global organization and in cooperation with PPD to assist in the development and execution critical strategic recruitment and employment programs that are efficient and responsive to the needs of the business. Principal Duties and Responsibilities (Essential Functions): Recruitment Process Optimization: Deploy best practices in recruiting, and innovative recruiting techniques best suited to the Evidera candidate pool. Stay informed of relevant industry issues, macro-economic labor markets and Evidera’s competitors for talent. Educate and train leaders, recruitment and HR team members on processes and practices for identifying, attracting, assessing, and closing qualified, diverse talent. Gather and report on crucial recruitment metrics (including client satisfaction and candidate experience), and devise strategies to make improvements where needed. Candidate Sourcing and Network Development: Leverage and optimize all available tools including internal and external networks, social media, job boards, direct sourcing, employee referrals and others. Develop and maintain strong business partnerships with company leaders and staff, vendors, community organizations, and institutions of higher education to identify and source candidates. Candidate Assessment: Devise and review selection criteria, assessment methods and operational procedures and processes to ensure relevance and efficiencies. Compliance: Ensure all hiring practices are in compliance with all US and international laws and regulations demonstrating a thorough understanding of pertinent legal protocol in hiring practices and completion of required government reporting. Branding: Partner with HR and Marketing to develop and promote a consistent and attractive employment brand across all channels. Hands-on Recruitment: Perform senior-level recruitment searches. Education, Professional Skills & Experience Undergraduate degree required, relevant professional certification strongly preferred. 10 years of success in full life cycle recruitment with significant experience recruiting for senior level roles. Experience in consulting environment with exposure to life sciences and/or the pharmaceutical industry strongly preferred Demonstrated success in using innovative means to attract talent in a highly competitive market and a highly competitive industry Experience working within an Affirmative Action plan and with immigration issues related to global hiring Expert use of MS Office and a commercially available ATS – experience with COMPAS or Taleo a plus Ability to create and monitor relevant recruitment metrics and report to management Ability to deliver on multiple and simultaneous competing priorities through individual, collaborative and delegated efforts with minimal direct supervision Superior written and verbal communication skills, including copywriting ability Excellent interpersonal skills including demonstrated success in quickly establishing and maintaining rapport and influencing decision-making across a wide variety of internal and external audiences Company Summary Evidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology. Perks Evidera offers a competitive salary and benefits package, with clear opportunities for growth and career progression. You will have the opportunity to work on multiple projects with some of the industry’s leading researchers. Our offices boast a fun and collaborative working environment, frequent social events and a robust support system. We are committed to providing training and professional development, with ample opportunity to advance, for all our staff. How to Apply Please complete your online profile by attaching your CV and covering letter addressing your suitability for the role. Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, sexual orientation, gender preference, disability, or status as a qualified individual with a disability or protected veteran.

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Director – Business Development – (Los Angeles, CA)

newabout 22 hours ago
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Director – Business Development – (Los Angeles, CA) Position Overview: This position provides direct business development, and sales and marketing support for Health Economics, Outcomes Research, Epidemiology, Real World Evidence, Medical Affairs research, and Global Market Access solutions to address our biopharma customer needs. This position reports to the Head of Global Business Development and focuses on identifying and securing new business in the biopharma sector. The Director is expected to work closely with Evidera's scientific, consulting and operational staff to present capabilities to clients, identify and qualify new business leads, maintain and manage relationships with key

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Senior Manager, Real World Evidence - Data Analytics

new1 day ago
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Senior Manager, Real World Evidence, Data Analytics – US East Coast , Bethesda preferred This is an exciting opportunity to join our successful research team and to help define and drive solutions for clients and patients. We are specifically recruiting someone for our Data Analytics team within Real-World Evidence to provide strategic oversight and project management support for a multi-million dollar program of research for one or more key accounts.This is a dynamic role involving regular contact with several key internal and sponsor stakeholders. The Team Evidera has been providing epidemiology, data analytics, and outcomes research services to clients in the biopharmaceutical industry for over 19 years. The Real-World Evidence team supports pharmaceutical, biotechnology and medical device companies in the design and conduct of real-world observational studies throughout the product lifecycle, from early pre-launch planning to launch and post-marketing management. Our focus is on helping our clients identify evidence gaps and rapidly build epidemiologic and economic evidence to demonstrate the effectiveness, safety and value of their products. For this role, the focus is on observational epidemiologic studies both retrospective and prospective in nature, targeted literature reviews, and risk management plans. Data collected in these studies is then used to address key research questions such as: Burden of disease and identification of unmet needs Treatment patterns, drug utilization, adherence Resource utilization The identification and impact of risk factors on disease outcomes Comparative effectiveness Safety outcomes We use epidemiologic methods to build knowledge of the relationships between patient, drug, clinical and disease factors that significantly aids our clients and the patients they serve in understanding health conditions and navigating potential drug-event causal relationships as well as in building stronger evidence-based value messages. Role and Responsibilities The Senior Project Manager reports to the Executive Director. He/she supports the Executive Sponsor in the strategic oversight and management of a diverse portfolio of work for one or more key accounts. This involves the collection, tracking, and processing of data to inform decision making, managing the day-to-day communication between the sponsor and internal stakeholders, ensuring project budgets and timelines are being managed appropriately, facilitation of internal and sponsor meetings to discuss strategic planning, business development, pipeline updates, share lessons learned, and enhance client service. In particular, the Senior Project Manager will: Be responsible for the overall coordination and management of administrative aspects of individual studies from receipt of lead through project set-up and delivery to the sponsor, including but not limited to financial and legal aspects of project management. Be responsible for financial stewardship and dashboard reporting of the account, per sponsor requirements. Work to ensure that all project deliverables meet the customer time/quality/cost expectations. Work with senior management and functional area leads to identify and evaluate fundamental issues on the project and ensure solutions are implemented. Able to escalate and communicate risks and concerns, as well as develop mitigation plans specific to project needs Oversee and manage diverse real-world evidence projects for multiple stakeholders within a key account; perform traditional project management activities such as ensuring all project deliverables, timelines, and budgets are closely monitored, as well as oversee Quality Control processes, ensure appropriate documentation of quality validation steps, oversee and manage third-party vendors, and keep relevant internal and sponsor stakeholders informed/consulted as appropriate. Contribute to the design and refinement of accounts-specific tools and processes as needed to meet or exceed client expectations with regards to account management. Support client communication, both providing key messaging to internal team members, but also disseminating study team communications to clients and external stakeholders Work across functional groups and departments to ensure successful delivery of studies, including but not limited to data analytics programmers and research scientists. Engage internal teams in discussions to share lessons learned, share ideas for improvement, and discuss strategic approach to Real-World Evidence positioning and business development. Support new sales opportunities including, but not limited to, budget development, proposal content development, and ‘win’ strategies Provide support for the Data Analytics Sr Leadership Team in defining and meeting specific business targets Identify opportunities to expand the account and enhance client service; propose solutions and recommendations both internally and to the sponsor directly. Work on site at client offices 40-60% of work week; regularly meet face-to-face with key client contacts to discuss status of ongoing studies, pipeline, and administrative topics. Qualifications and Experience Bachelor’s degree or licensed certified health care training or equivalent combination of education and experience that provides the individual with the required knowledge, skills and abilities. Project management certification (e.g. PMP, PgMP, CAPM) or demonstration of project management skills including scope, budgeting, forecasting, timelines, resource management, and use of project management systems (e.g. MS Project). Demonstrable experience managing across a range of cross-functional, global, external stakeholders. A demonstrated track record of project managing a variety of studies within ideally either a CRO or consulting firm A deep understanding of the Life Science industry In depth understanding of observational projects and project portfolio management Strong written and verbal communication Proven ability to multitask and problem solve Excellent client facing skills Valid Passport, where appropriate. The position is permanent, full time and optimally based in Bethesda; 40-60% working on-site at sponsor’s office. Company Summary Evidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science, operational excellence, and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology. Why Choose Evidera? Evidera offers a competitive salary and benefits package. Our Bethesda office is conveniently located a few blocks from the Bethesda metro, local shops, and restaurants. This office also offers complimentary coffee & tea, breakfast on Fridays, frequent social events, and a spacious, quiet work environment. We are committed to providing training and professional development, with ample opportunity to advance for all our staff. The Real-World Evidence team constitutes a vibrant and dynamic group of individuals who specialize in scientific methods and research operations. Our mission is to be the global leader in generating and communicating evidence of product value to inform healthcare decision making. Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color , religion, sex, national origin, age, genetics, sexual orientation, gender preference disability, or status as a qualified individual with a disability or protected veteran.

Senior Global Recruiter Human Resources (Waltham, MA or Bethesda, MD) - Evidera

new1 day ago
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Senior Global Recruiter – Human Resources (Waltham, MA or Bethesda, MD) Position Overview: Reporting to the Executive Director of Global Recruitment, serves as a senior point of contact within assigned practice areas of Evidera’s talent acquisition program. The incumbent works across the global organization and in cooperation with PPD to assist in the development and execution critical strategic recruitment and employment programs that are efficient and responsive to the needs of the business. Principal Duties and Responsibilities (Essential Functions): Recruitment Process Optimization: Deploy best practices in recruiting, and innovative recruiting techniques best suited to the Evidera candidate pool. Stay informed of relevant industry issues, macro-economic labor markets and Evidera’s competitors for talent. Educate and train leaders, recruitment and HR team members on processes and practices for identifying, attracting, assessing, and closing qualified, diverse talent. Gather and report on crucial recruitment metrics (including client satisfaction and candidate experience), and devise strategies to make improvements where needed. Candidate Sourcing and Network Development: Leverage and optimize all available tools including internal and external networks, social media, job boards, direct sourcing, employee referrals and others. Develop and maintain strong business partnerships with company leaders and staff, vendors, community organizations, and institutions of higher education to identify and source candidates. Candidate Assessment: Devise and review selection criteria, assessment methods and operational procedures and processes to ensure relevance and efficiencies. Compliance: Ensure all hiring practices are in compliance with all US and international laws and regulations demonstrating a thorough understanding of pertinent legal protocol in hiring practices and completion of required government reporting. Branding: Partner with HR and Marketing to develop and promote a consistent and attractive employment brand across all channels. Hands-on Recruitment: Perform senior-level recruitment searches. Education, Professional Skills & Experience Undergraduate degree required, relevant professional certification strongly preferred. 10 years of success in full life cycle recruitment with significant experience recruiting for senior level roles. Experience in consulting environment with exposure to life sciences and/or the pharmaceutical industry strongly preferred Demonstrated success in using innovative means to attract talent in a highly competitive market and a highly competitive industry Experience working within an Affirmative Action plan and with immigration issues related to global hiring Expert use of MS Office and a commercially available ATS – experience with COMPAS or Taleo a plus Ability to create and monitor relevant recruitment metrics and report to management Ability to deliver on multiple and simultaneous competing priorities through individual, collaborative and delegated efforts with minimal direct supervision Superior written and verbal communication skills, including copywriting ability Excellent interpersonal skills including demonstrated success in quickly establishing and maintaining rapport and influencing decision-making across a wide variety of internal and external audiences Company Summary Evidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology. Perks Evidera offers a competitive salary and benefits package, with clear opportunities for growth and career progression. You will have the opportunity to work on multiple projects with some of the industry’s leading researchers. Our offices boast a fun and collaborative working environment, frequent social events and a robust support system. We are committed to providing training and professional development, with ample opportunity to advance, for all our staff. How to Apply Please complete your online profile by attaching your CV and covering letter addressing your suitability for the role. Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, sexual orientation, gender preference, disability, or status as a qualified individual with a disability or protected veteran.

Research Associate I - Modeling and Simulation

new1 day ago
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Research Associate I - Modeling and Simulation Our multidisciplinary Modeling and Simulation experts design and implement health economic models that describe complex medical processes to understand and evaluate the implications of clinical trials; demonstrate the value of interventions beyond efficacy, and assess benefits, risks, and the economic consequences associated with healthcare interventions. If you have a passion for health economic modeling to conduct cost-effectiveness analyses of healthcare interventions and have experience conceptualizing and implementing simulation models (e.g., discrete event simulation) and other decision-analytic models (e.g., decision trees, Markov, individual state-transition, survival partition), a position in Modeling and Simulation at Evidera is waiting for you Position Overview Assist with implementing simulation models (e.g., discrete event simulation) and other decision-analytic models (e.g., Markov, individual state-transition, survival partition) to assess the cost-effectiveness of healthcare interventions. Assist with scientific and financial project management, and monitoring progress for projects when assigned. Essential Duties and Responsibilities: (other duties may be assigned) Assist with implementing one or more of the following (under supervision): Development of health economic models to conduct cost-effectiveness and budget impact analyses of healthcare interventions. Program models using Microsoft Excel with Visual Basic for Applications (VBA). Conduct analyses and presentation of results. Conduct literature reviews with emphasis on extracting data pertinent to health economic evaluations and cost-effectiveness analyses. Conduct basic statistical analyses (e.g., descriptive statistics and regression analysis). Assist with drafting sections of project deliverables (e.g., user guides, model specifications and technical reports). Participate in client meetings and draft meeting minutes. Assist with tracking budget and expenses and monitoring timelines and deliverables for projects when assigned. Support other "non-billable" activities as needed (e.g., assist with developing sections of proposals). Travel may be required. Education and Experience Master’s degree in Health Economics, Mathematics, or Epidemiology with more than one year of relevant work experience. Master’s or Bachelor’s degrees in other fields will be considered (e.g. Operations Research or Industrial Engineering) with relevant experience of programming decision analytic models (e.g. decision trees, Markov, survival partition) in Microsoft Excel with VBA. What you bring to Evidera Basic understanding of research methods. Practical knowledge of research project implementation. Experience working with modeling/simulation software, in particular Microsoft Excel using VBA. Excellent computer skills, including Microsoft Word and PowerPoint. Strong quantitative skills, with solid understanding of basic statistics. Energy, a great work attitude and fit well with our team. Strong organization skills. Language Skills Competent in written and spoken English. Computer Skills Required: Excel and VBA expertise, Microsoft Word, Microsoft PowerPoint Desired: Experience using other simulation and/or decision-analysis software (e.g., Arena, TreeAge). Company Summary Evidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology. Why Choose Evidera? Evidera offers a competitive salary and benefits package, with clear opportunities for growth and career progression. You will have the opportunity to work on multiple projects with some of the industry’s leading researchers. Our offices boast a fun and collaborative working environment, frequent social events and a robust support system. We are committed to providing training and professional development, with ample opportunity to advance, for all our staff. Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, sexual orientation, gender preference disability, or status as a qualified individual with a disability or protected veteran.

Associate Counsel (Contracts) Legal (Bethesda, MD or

new1 day ago
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Associate Counsel (Contracts) – Legal (Bethesda, MD or Wilmington, NC)Position Overview:Provides legal advice and support in the drafting, review and negotiation of agreements with minimal oversight. Serves as the primary contact (within the department and with internal and external customers) for agreements assigned to their group while working autonomously. Ensures that Evidera/PPD's best interests are protected at all times and that senior and executive management have the legal information necessary to make informed decisions and grant approvals for business risks. Assists with customer disputes as requested.Principal Duties and Responsibilities:With oversight, provides legal advice and represents PPD in legal matters.Prepares, negotiates and finalizes PPD Agreements and/or other related documentation.Assesses legal risks and provides recommendations and alternative mitigating resolutions to departmental and senior management.Makes recommendations to Executive Management with regard to risks, strategies and recommendations upon request.Participates in committees as needed.Provides training to other functional groups within PPD on contract requirements and other legal matters.Develops processes and training and takes advantage of other departmental improvement opportunities.Understands and adheres to Evidera/PPD and Client SOPs, WPDs and other regulations for all aspects of project implementation, execution and closeout.Assists in other legal matters, as required.Education, Professional Skills & Experience Bachelor's degree and advanced degree in law (juris doctorate or equivalent educational model in other jurisdictions).Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years); or an equivalent combination of education, training, & experience.Personal Skills & Competencies Excellent communication and interpersonal skillsSubstantial organizational skills and strong attention to detail with proven ability to handle multiple tasks efficiently and effectivelyMust be flexible and able to reprioritize workload to meet changing project needsComprehensive MS Excel and MS Word skillsExcellent English and grammar skillsExcellent analytical and decision-based thinkingCapable of drafting and negotiating routine contract provisions autonomously and complex contract provisions, with oversightMust be able to work independently and as a team playerMust be able to identify risk and evaluate fact patterns to advise on the application of the law (may require some oversight)Ability to apply knowledge of and adhere to all PPD and Client SOPs, WPDs and other regulations in all aspects of project implementation, execution and closeoutAbility to identify legal risks and develop strategic and tactical ways to minimize such risksCompany SummaryEvidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology.PerksEvidera offers a competitive salary and benefits package, with clear opportunities for growth and career progression. You will have the opportunity to work on multiple projects with some of the industry’s leading researchers. Our offices boast a fun and collaborative working environment, frequent social events and a robust support system. We are committed to providing training and professional development, with ample opportunity to advance, for all our staff.How to ApplyPlease complete your online profile by attaching your CV and covering letter addressing your suitability for the role.Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, sexual orientation, gender preference,disability, or status as a qualified individual with a disability or protected veteran.

Senior Global Recruiter Human Resources (Waltham, MA or Bethesda, MD) - Evidera

new1 day ago
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Senior Global Recruiter – Human Resources (Waltham, MA or Bethesda, MD)Position Overview:Reporting to the Executive Director of Global Recruitment, serves as a senior point of contact within assigned practice areas of Evidera’s talent acquisition program. The incumbent works across the global organization and in cooperation with PPD to assist in the development and execution critical strategic recruitment and employment programs that are efficient and responsive to the needs of the business.Principal Duties and Responsibilities (Essential Functions**):Recruitment Process Optimization: Deploy best practices in recruiting, and innovative recruiting techniques best suited to the Evidera candidate pool. Stay informed of relevant industry issues, macro-economic labor markets and Evidera’s competitors for talent. Educate and train leaders, recruitment and HR team members on processes and practices for identifying, attracting, assessing, and closing qualified, diverse talent. Gather and report on crucial recruitment metrics (including client satisfaction and candidate experience), and devise strategies to make improvements where needed.Candidate Sourcing and Network Development: Leverage and optimize all available tools including internal and external networks, social media, job boards, direct sourcing, employee referrals and others. Develop and maintain strong business partnerships with company leaders and staff, vendors, community organizations, and institutions of higher education to identify and source candidates. Candidate Assessment: Devise and review selection criteria, assessment methods and operational procedures and processes to ensure relevance and efficiencies.Compliance: Ensure all hiring practices are in compliance with all US and international laws and regulations demonstrating a thorough understanding of pertinent legal protocol in hiring practices and completion of required government reporting.Branding: Partner with HR and Marketing to develop and promote a consistent and attractive employment brand across all channels.Hands-on Recruitment: Perform senior-level recruitment searches.Education, Professional Skills & Experience Undergraduate degree required, relevant professional certification strongly preferred.10 years of success in full life cycle recruitment with significant experience recruiting for senior level roles.Experience in consulting environment with exposure to life sciences and/or the pharmaceutical industry strongly preferredDemonstrated success in using innovative means to attract talent in a highly competitive market and a highly competitive industryExperience working within an Affirmative Action plan and with immigration issues related to global hiring Expert use of MS Office and a commercially available ATS – experience with COMPAS or Taleo a plusAbility to create and monitor relevant recruitment metrics and report to managementAbility to deliver on multiple and simultaneous competing priorities through individual, collaborative and delegated efforts with minimal direct supervisionSuperior written and verbal communication skills, including copywriting abilityExcellent interpersonal skills including demonstrated success in quickly establishing and maintaining rapport and influencing decision-making across a wide variety of internal and external audiencesCompany SummaryEvidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology.PerksEvidera offers a competitive salary and benefits package, with clear opportunities for growth and career progression. You will have the opportunity to work on multiple projects with some of the industry’s leading researchers. Our offices boast a fun and collaborative working environment, frequent social events and a robust support system. We are committed to providing training and professional development, with ample opportunity to advance, for all our staff.How to ApplyPlease complete your online profile by attaching your CV and covering letter addressing your suitability for the role.Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, sexual orientation, gender preference, disability, or status as a qualified individual with a disability or protected veteran.

Senior Research Associate Meta Research (Waltham, MA or London, UK) - Evidera

new1 day ago
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Senior Research Associate – Meta Research We are looking to fill this role in our Waltham, MA or London, UK offices; however, we will consider other locations based on the candidates’ experience and qualificationsThe TeamDo you have what it takes to conduct high-quality systematic literature reviews (SLRs)? Just about anyone seeking published articles to answer research questions can type terms into a database and then hope to make sense of the information retrieved. But when done without the right knowledge, skills, and experience, such an exercise risks answers that are biased, confusing, incomplete, or wholly incorrect. Poorly designed search algorithms, unworkable PICOS criteria and failure to follow PRISMA study-reporting guidelines are just a few of many things that often go wrong with such attempts at literature reviewing. This helps explain what makes Meta Research different. Our SLRs and related meta-analyses reflect broad clinical knowledge and expertise in finding and assessing complex information. This means our clients and Evidera colleagues can rely on us to discover, synthesize, and contextualize the data that really matter and thereby provide them with insights they could not have obtained by themselves. Here are just some of the things our SLRs help our clients and colleagues to do:Understand new indications in context of specific product strategyInform planning for primary research, such as choice of patient-reported outcome instruments and comparatorsEstimate clinical comparisons of products versus competitorsCapitalize on existing research while assessing evidence gapsProvide information for value development planningDetermine which databases have proved useful in target indicationsDerive model inputsCreate burden-of-illness assessments for submission to payersPublish burden assessments for disseminationPopulate dossiersPopulate regulatory documents such as Risk Management Plans.The RoleWe are looking for a Senior Research Associate (Systematic Literature Reviews) for our Meta Research team in our Waltham, MA or London, UK offices. This role will independently direct key aspects of systematic literature review (SLR) research projects with guidance from senior staff, as well as manage multiple projects with tasks varying to degree by project.ResponsibilitiesHave co-PI/working-PI responsibilities (share project oversight with PI) or may serve as Project Manager on highly complex projects or programs of workDelegate tasks and monitors progress of delegated project tasksDesign/responsible for study – quantitative and qualitative – or share responsibility with PI (e.g., systematic review strategy and protocols, SAPs, etc)Responsible for study implementation and data analysisReview study inclusion/exclusionReview study data extractionInterpret results; edit to finalize resultsPresent findings or advise on presentationBegin to undertake strategic planning tasks with PI/research scientistsReview/edit to finalize draft project deliverablesAuthor/edit/review abstracts/posters/manuscriptsMaintain familiarity with current scientific literature. Author presentations for scientific conferences and manuscripts for scientific journals.Becoming active in professional organizationsUndertake other scientific tasks as assignedResponsible for project management of large projectsDelegate project managementResponsible for client communication and problem solving with PIKnow project management systems (electronic and paper filing, SOP requirements, Finance office practices, etc.) and implement as requiredIf project PI, have financial responsibility for projectSupport PI/research scientists in scientific tasks for business developmentDesign proposals and review draftsManage and alert PI to scope of work changesInteract with clients to win new business and identify business leadsParticipate in staff recruitment efforts (phone screening, interviewing, attending presentations, etc.)Conform to SOPs and other Evidera requirementsConduct and participate in the training of junior staff and new hiresFulfill the tasks associated with the role of supervisorProvide formal or informal leadership, oversight, mentoring, and guidance to junior staffQualificationsand ExperiencePhD in health sciences, economics, biology, natural sciences or a related field with some related experience; MSc. with significant related experience, or Bachelors with extensive related experienceProven experience in systematic literature review methods in health economics and/or health services research; experience in network meta-analysis would be an advantage, but is not essentialCommercial experience in a similar environment is highly desirable, but not essentialDeep understanding of research principles and demonstrated practical research implementationCompany SummaryEvidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology.Why Choose Evidera?Evidera offers a competitive salary and benefits package. We are committed to providing training and professional development, with ample opportunity to advance for all of our staff. Both our Waltham and London offices are conveniently located close to transport links, local shops, and restaurants. In addition, both offices offer complimentary coffee & tea, breakfast on Fridays, frequent social events, and a spacious, quiet work environment. Our mission is to be the global leader in generating and communicating evidence of product value to inform healthcare decision making.How to ApplyTo apply, please complete your online profile by attaching your CV and covering letter addressing your suitability for the role. All applications are reviewed, and qualified candidates will be contacted. Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, sexual orientation, gender preference, disability, or status as a qualified individual with a disability or protected veteran.

Associate Counsel (Contracts) Legal (Bethesda, MD or

new2 days ago
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Associate Counsel (Contracts) – Legal (Bethesda, MD or Wilmington, NC) Position Overview: Provides legal advice and support in the drafting, review and negotiation of agreements with minimal oversight. Serves as the primary contact (within the department and with internal and external customers) for agreements assigned to their group while working autonomously. Ensures that Evidera/PPD's best interests are protected at all times and that senior and executive management have the legal information necessary to make informed decisions and grant approvals for business risks. Assists with customer disputes as requested. Principal Duties and Responsibilities: With oversight, provides legal advice and represents PPD in legal matters. Prepares, negotiates and finalizes PPD Agreements and/or other related documentation. Assesses legal risks and provides recommendations and alternative mitigating resolutions to departmental and senior management. Makes recommendations to Executive Management with regard to risks, strategies and recommendations upon request. Participates in committees as needed. Provides training to other functional groups within PPD on contract requirements and other legal matters. Develops processes and training and takes advantage of other departmental improvement opportunities. Understands and adheres to Evidera/PPD and Client SOPs, WPDs and other regulations for all aspects of project implementation, execution and closeout. Assists in other legal matters, as required. Education, Professional Skills & Experience Bachelor's degree and advanced degree in law (juris doctorate or equivalent educational model in other jurisdictions). Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years); or an equivalent combination of education, training, & experience. Personal Skills & Competencies Excellent communication and interpersonal skills Substantial organizational skills and strong attention to detail with proven ability to handle multiple tasks efficiently and effectively Must be flexible and able to reprioritize workload to meet changing project needs Comprehensive MS Excel and MS Word skills Excellent English and grammar skills Excellent analytical and decision-based thinking Capable of drafting and negotiating routine contract provisions autonomously and complex contract provisions, with oversight Must be able to work independently and as a team player Must be able to identify risk and evaluate fact patterns to advise on the application of the law (may require some oversight) Ability to apply knowledge of and adhere to all PPD and Client SOPs, WPDs and other regulations in all aspects of project implementation, execution and closeout Ability to identify legal risks and develop strategic and tactical ways to minimize such risks Company Summary Evidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology. Perks Evidera offers a competitive salary and benefits package, with clear opportunities for growth and career progression. You will have the opportunity to work on multiple projects with some of the industry’s leading researchers. Our offices boast a fun and collaborative working environment, frequent social events and a robust support system. We are committed to providing training and professional development, with ample opportunity to advance, for all our staff. How to Apply Please complete your online profile by attaching your CV and covering letter addressing your suitability for the role. Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, sexual orientation, gender preference, disability, or status as a qualified individual with a disability or protected veteran.

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Senior Global Recruiter Human Resources (Waltham, MA or Bethesda, MD) - Evidera

new2 days ago
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Senior Global Recruiter - Human Resources (Waltham, MA or Bethesda, MD)Position Overview:Reporting to the Executive Director of Global Recruitment, serves as a senior point of contact within assigned practice areas of Evidera's talent acquisition program.The incumbent works across the global organization and in cooperation with PPD to assist in the development and execution critical strategic recruitment and employment programs that are efficient and responsive to the needs of the business.Pri

Senior Research Associate Meta Research (Waltham, MA or London, UK) - Evidera

new2 days ago
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Senior Research Associate - Meta Research We are looking to fill this role in our Waltham, MA or London, UK offices; however, we will consider other locations based on the candidates' experience and qualifications The Team Do you have what it takes to conduct high-quality systematic literature reviews (SLRs)? Just about anyone seeking published articles to answer research questions can type terms into a database and then hope to make sense of the information retrieved.But when done without the

Research Associate I - Modeling and Simulation

new2 days ago
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Research Associate I - Modeling and Simulation Our multidisciplinary Modeling and Simulation experts design and implement health economic models that describe complex medical processes to understand and evaluate the implications of clinical trials; demonstrate the value of interventions beyond efficacy, and assess benefits, risks, and the economic consequences associated with healthcare interventions. If you have a passion for health economic modeling to conduct cost-effectiveness analyses of healthcare interventions and have experience conceptualizing and implementing simulation models (e.g., discrete event simulation) and other decision-analytic models (e.g., decision trees, Markov, individual state-transition, survival partition), a position in Modeling and Simulation at Evidera is waiting for you Position Overview Assist with implementing simulation models (e.g., discrete event simulation) and other decision-analytic models (e.g., Markov, individual state-transition, survival partition) to assess the cost-effectiveness of healthcare interventions. Assist with scientific and financial project management, and monitoring progress for projects when assigned. Essential Duties and Responsibilities: (other duties may be assigned) Assist with implementing one or more of the following (under supervision): Development of health economic models to conduct cost-effectiveness and budget impact analyses of healthcare interventions. Program models using Microsoft Excel with Visual Basic for Applications (VBA). Conduct analyses and presentation of results. Conduct literature reviews with emphasis on extracting data pertinent to health economic evaluations and cost-effectiveness analyses. Conduct basic statistical analyses (e.g., descriptive statistics and regression analysis). Assist with drafting sections of project deliverables (e.g., user guides, model specifications and technical reports). Participate in client meetings and draft meeting minutes. Assist with tracking budget and expenses and monitoring timelines and deliverables for projects when assigned. Support other "non-billable" activities as needed (e.g., assist with developing sections of proposals). Travel may be required. Education and Experience Master’s degree in Operations Research or Industrial Engineering or Bachelor’s degree in Operations Research or Industrial Engineering with more than one year of relevant work experience. Master’s or Bachelor’s degrees in other fields will be considered (e.g., Mathematics, Economics, Epidemiology) with relevant experience of programming decision analytic models (e.g., decision trees, Markov, individual state-transition, survival partition) in Microsoft Excel with VBA. What you bring to Evidera Basic understanding of research methods. Practical knowledge of research project implementation. Experience working with modeling/simulation software, in particular Microsoft Excel using VBA. Excellent computer skills, including Microsoft Word and PowerPoint. Strong quantitative skills, with solid understanding of basic statistics. Energy, a great work attitude and fit well with our team. Strong organization skills. Language Skills Competent in written and spoken English. Computer Skills Required: Excel and VBA expertise, Microsoft Word, Microsoft PowerPoint Desired: Experience using other simulation and/or decision-analysis software (e.g., Arena, TreeAge). Company Summary Evidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology. Why Choose Evidera? Evidera offers a competitive salary and benefits package. We are committed to providing training and professional development, with ample opportunity to advance for all of our staff. Both our Waltham and London offices are conveniently located close to transport links, local shops, and restaurants. In addition, both offices offer complimentary coffee & tea, breakfast on Fridays, frequent social events, and a spacious, quiet work environment. Our mission is to be the global leader in generating and communicating evidence of product value to inform healthcare decision making. Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, sexual orientation, gender preference disability, or status as a qualified individual with a disability or protected veteran.

Senior Research Associate Meta Research (Waltham, MA or London, UK)

5 days ago
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Senior Research Associate – Meta Research We are looking to fill this role in our Waltham, MA or London, UK offices; however, we will consider other locations based on the candidates’ experience and qualifications The Team Do you have what it takes to conduct high-quality systematic literature reviews (SLRs)? Just about anyone seeking published articles to answer research questions can type terms into a database and then hope to make sense of the information retrieved. But when done without the right knowledge, skills, and experience, such an exercise risks answers that are biased, confusing, incomplete, or wholly incorrect. Poorly designed search algorithms, unworkable PICOS criteria and failure to follow PRISMA study-reporting guidelines are just a few of many things that often go wrong with such attempts at literature reviewing. This helps explain what makes Meta Research different. Our SLRs and related meta-analyses reflect broad clinical knowledge and expertise in finding and assessing complex information. This means our clients and Evidera colleagues can rely on us to discover, synthesize, and contextualize the data that really matter and thereby provide them with insights they could not have obtained by themselves. Here are just some of the things our SLRs help our clients and colleagues to do: Understand new indications in context of specific product strategy Inform planning for primary research, such as choice of patient-reported outcome instruments and comparators Estimate clinical comparisons of products versus competitors Capitalize on existing research while assessing evidence gaps Provide information for value development planning Determine which databases have proved useful in target indications Derive model inputs Create burden-of-illness assessments for submission to payers Publish burden assessments for dissemination Populate dossiers Populate regulatory documents such as Risk Management Plans. The Role We are looking for a Senior Research Associate (Systematic Literature Reviews) for our Meta Research team in our Waltham, MA or London, UK offices. This role will independently direct key aspects of systematic literature review (SLR) research projects with guidance from senior staff, as well as manage multiple projects with tasks varying to degree by project. Responsibilities Have co-PI/working-PI responsibilities (share project oversight with PI) or may serve as Project Manager on highly complex projects or programs of work Delegate tasks and monitors progress of delegated project tasks Design/responsible for study – quantitative and qualitative – or share responsibility with PI (e.g., systematic review strategy and protocols, SAPs, etc) Responsible for study implementation and data analysis Review study inclusion/exclusion Review study data extraction Interpret results; edit to finalize results Present findings or advise on presentation Begin to undertake strategic planning tasks with PI/research scientists Review/edit to finalize draft project deliverables Author/edit/review abstracts/posters/manuscripts Maintain familiarity with current scientific literature. Author presentations for scientific conferences and manuscripts for scientific journals. Becoming active in professional organizations Undertake other scientific tasks as assigned Responsible for project management of large projects Delegate project management Responsible for client communication and problem solving with PI Know project management systems (electronic and paper filing, SOP requirements, Finance office practices, etc.) and implement as required If project PI, have financial responsibility for project Support PI/research scientists in scientific tasks for business development Design proposals and review drafts Manage and alert PI to scope of work changes Interact with clients to win new business and identify business leads Participate in staff recruitment efforts (phone screening, interviewing, attending presentations, etc.) Conform to SOPs and other Evidera requirements Conduct and participate in the training of junior staff and new hires Fulfill the tasks associated with the role of supervisor Provide formal or informal leadership, oversight, mentoring, and guidance to junior staff Qualifications and Experience PhD in health sciences, economics, biology, natural sciences or a related field with some related experience; MSc. with significant related experience, or Bachelors with extensive related experience Proven experience in systematic literature review methods in health economics and/or health services research; experience in network meta-analysis would be an advantage, but is not essential Commercial experience in a similar environment is highly desirable, but not essential Deep understanding of research principles and demonstrated practical research implementation Company Summary Evidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology. Why Choose Evidera? Evidera offers a competitive salary and benefits package. We are committed to providing training and professional development, with ample opportunity to advance for all of our staff. Both our Waltham and London offices are conveniently located close to transport links, local shops, and restaurants. In addition, both offices offer complimentary coffee & tea, breakfast on Fridays, frequent social events, and a spacious, quiet work environment. Our mission is to be the global leader in generating and communicating evidence of product value to inform healthcare decision making. How to Apply To apply, please complete your online profile by attaching your CV and covering letter addressing your suitability for the role. All applications are reviewed, and qualified candidates will be contacted. Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, sexual orientation, gender preference, disability, or status as a qualified individual with a disability or protected veteran.

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Senior Systematic Reviewer (Research Associate III) Meta Research (Waltham MA or London UK)

7 days ago
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Senior Systematic Reviewer (Research Associate III) – Meta Research (Waltham MA or London UK) We are looking to fill this role in our Waltham, MA or London, UK offices The Team Do you have what it takes to conduct high-quality systematic literature reviews (SLRs)? Just about anyone seeking published articles to answer research questions can type terms into a database and then hope to make sense of the information retrieved. But when done without the right knowledge, skills, and experience, such an exercise risks answers that are biased, confusing, incomplete, or wholly incorrect. Poorly designed search algorithms, unworkable PICOS criteria and failure to follow PRISMA study-reporting guidelines are just a few of many things that often go wrong with such attempts at literature reviewing. This helps explain what makes Meta Research different. Our SLRs and related meta-analyses reflect broad clinical knowledge and expertise in finding and assessing complex information. This means our clients and Evidera colleagues can rely on us to discover, synthesize, and contextualize the data that really matter and thereby provide them with insights they could not have obtained by themselves. Here are just some of the things our SLRs help our clients and colleagues to do: Understand new indications in context of specific product strategy Inform planning for primary research, such as choice of patient-reported outcome instruments and comparators Estimate clinical comparisons of products versus competitors Capitalize on existing research while assessing evidence gaps Provide information for value development planning Determine which databases have proved useful in target indications Derive model inputs Create burden-of-illness assessments for submission to payers Publish burden assessments for dissemination Populate dossiers Populate regulatory documents such as Risk Management Plans. The Role We are looking for a Research Associate III (Senior Systematic Reviewer) for our Meta Research team in our Waltham, MA or London, UK offices. This role will independently direct key aspects of systematic literature review (SLR) research projects with guidance from senior staff, as well as manage multiple projects with tasks varying to degree by project. Responsibilities : Define and refine research questions as they pertain to the SLR objectives Design of literature searches/algorithms to be implemented in scientific literature databases (i.e., PubMed, EMBASE, Cochrane Library, etc.) and grey literature sources (conference proceedings, regulatory agencies). Develop inclusion/exclusion criteria within the PICOS framework to be implemented during screening process Oversee the screening of abstracts and full-text articles against defined inclusion/exclusion criteria to assess their suitability for inclusion in the review Review the PRISMA diagram depicting the study attrition Validate data abstraction and extraction Finalize the analyzable dataset Draft tables and figures for analysis results Synthesize the evidence base by through drafting and editing sections of project deliverables (e.g. reports, protocols, statistical analysis plans) and dissemination actives, abstract and manuscript preparation Delegate tasks to junior staff and review their work as appropriate Develop a project plan and monitor project progress, including timeline and budget Draft project proposals, including scoping the body of evidence and preparing project budgets) Co-lead (or lead) client communications, both via email, phone, and in-person; responsible for day-to-day communications Participate in non-literature based research and consulting activities within other departments (e.g., modeling and simulation, real-world evidence). Participate in staff recruitment and training efforts Serve as a line manager (depending on skills/experience) Qualifications and Experience PhD in health sciences, economics, biology, natural sciences or a related field with some related experience; MSc. with significant related experience, or Bachelors with extensive related experience Proven experience in systematic literature review methods in health economics and/or health services research; experience in network meta-analysis would be an advantage, but is not essential Commercial experience in a similar environment is highly desirable, but not essential Deep understanding of research principles and demonstrated practical research implementation Company Summary Evidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology. Why Choose Evidera? Evidera offers a competitive salary and benefits package. We are committed to providing training and professional development, with ample opportunity to advance for all of our staff. Both our Waltham and London offices are conveniently located close to transport links, local shops, and restaurants. In addition, both offices offer complimentary coffee & tea, breakfast on Fridays, frequent social events, and a spacious, quiet work environment. Our mission is to be the global leader in generating and communicating evidence of product value to inform healthcare decision making. How to Apply To apply, please complete your online profile by attaching your CV and covering letter addressing your suitability for the role. All applications are reviewed, and qualified candidates will be contacted. Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color , religion, sex, national origin, age, genetics, sexual orientation, gender preference disability, or status as a qualified individual with a disability or protected veteran.

jobs byAdzuna

Executive Director, Integrated Solutions - Real-World Evidence (Flexible Location)

11 days ago
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Position Summary The Executive Director, Integrated RWE Solutions is a senior leader within Peri- and Post-Approval Studies (PPAS) group, responsible for the performance, growth and development of integrated RWE solutions. PPAS consists of three distinct practice areas: Interventional Studies, Non-Interventional Studies (NIS) and Data Analytics (DA), with the latter two practices forming Evidera’s RWE solutions. Through deep understanding of client needs and the ecosystem of RWE offerings, the incumbent works closely with PPAS business leadership to advance Evidera market position and support the achievement of Company level authorizations, revenue and profit goals. The Executive Direc

jobs byAdzuna

Managing Director, Real World Value and Strategy Consulting

11 days ago
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Managing Director, Real World Value and Strategy Consulting – Peri and Post Approval Studies (Flexible) Position Overview: Evidera’s Real World Value and Strategy (RVS) team within Peri- and Post-Approval Studies group focuses on ensuring that scientific and operational excellence come together to help optimize life sciences manufacturer strategic clinical, regulatory, access and commercial business objectives. We blend proven global RWE operational and scientific excellence with world class market access, regulatory consulting and real-world evidence expertise to impact acceptance and uptake. Our strategic focus ensures that our RWE partnership model is focused on our client’s most impo

jobs byAdzuna

Senior Manager/Associate Director - Marketing (Flexible)

13 days ago
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Senior Manager/Associate Director - Marketing (Flexible) Position Overview Evidera is seeking a talented and energetic marketing professional to assist with a wide variety of projects and promotional efforts. Responsibilities will include designing and managing marketing campaigns, creating content for various marketing pieces, managing and tracking advertisements, assisting with digital marketing efforts, and other marketing activities to support brand awareness and new lead generation. As an experienced marketing expert, you will play a major role in helping the team develop proactive marketing strategies, launch and promote new offerings, and develop engaging and persuasive messagin

jobs byAdzuna

Managing Director, Real World Value and Strategy Consulting – Peri and Post Approval Studies (Flexible)

13 days ago
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Managing Director, Real World Value and Strategy Consulting – Peri and Post Approval Studies (Flexible) Position Overview: Evidera’s Real World Value and Strategy (RVS) team within Peri- and Post-Approval Studies group focuses on ensuring that scientific and operational excellence come together to help optimize life sciences manufacturer strategic clinical, regulatory, access and commercial business objectives. We blend proven global RWE operational and scientific excellence with world class market access, regulatory consulting and real-world evidence expertise to impact acceptance and uptake. Our strategic focus ensures that our RWE partnership model is focused on our client’s most impo

jobs byAdzuna

Managing Director, Real World Value and Strategy Consulting – Peri and Post Approval Studies (Flexible)

13 days ago
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Managing Director, Real World Value and Strategy Consulting – Peri and Post Approval Studies (Flexible) Position Overview: Evidera’s Real World Value and Strategy (RVS) team within Peri- and Post-Approval Studies group focuses on ensuring that scientific and operational excellence come together to help optimize life sciences manufacturer strategic clinical, regulatory, access and commercial business objectives. We blend proven global RWE operational and scientific excellence with world class market access, regulatory consulting and real-world evidence expertise to impact acceptance and uptake. Our strategic focus ensures that our RWE partnership model is focused on our client’s most impo

jobs byAdzuna

Managing Director, Real World Value and Strategy Consulting – Peri and Post Approval Studies (Flexible)

13 days ago
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Managing Director, Real World Value and Strategy Consulting – Peri and Post Approval Studies (Flexible) Position Overview: Evidera’s Real World Value and Strategy (RVS) team within Peri- and Post-Approval Studies group focuses on ensuring that scientific and operational excellence come together to help optimize life sciences manufacturer strategic clinical, regulatory, access and commercial business objectives. We blend proven global RWE operational and scientific excellence with world class market access, regulatory consulting and real-world evidence expertise to impact acceptance and uptake. Our strategic focus ensures that our RWE partnership model is focused on our client’s most impo

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Senior Manager, Real World Evidence - Data Analytics

16 days ago
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Senior Manager, Real World Evidence, Data Analytics – US East Coast , Bethesda preferred This is an exciting opportunity to join our successful research team and to help define and drive solutions for clients and patients. We are specifically recruiting someone for our Data Analytics team within Real-World Evidence to provide strategic oversight and project management support for a multi-million dollar program of research for one or more key accounts.This is a dynamic role involving regular contact with several key internal and sponsor stakeholders. The Team Evidera has been providing epidemiology, data analytics, and outcomes research services to clients in the biopharmaceutical industry for over 19 years. The Real-World Evidence team supports pharmaceutical, biotechnology and medical device companies in the design and conduct of real-world observational studies throughout the product lifecycle, from early pre-launch planning to launch and post-marketing management. Our focus is on helping our clients identify evidence gaps and rapidly build epidemiologic and economic evidence to demonstrate the effectiveness, safety and value of their products. For this role, the focus is on observational epidemiologic studies both retrospective and prospective in nature, targeted literature reviews, and risk management plans. Data collected in these studies is then used to address key research questions such as: Burden of disease and identification of unmet needs Treatment patterns, drug utilization, adherence Resource utilization The identification and impact of risk factors on disease outcomes Comparative effectiveness Safety outcomes We use epidemiologic methods to build knowledge of the relationships between patient, drug, clinical and disease factors that significantly aids our clients and the patients they serve in understanding health conditions and navigating potential drug-event causal relationships as well as in building stronger evidence-based value messages. Role and Responsibilities The Senior Project Manager reports to the Executive Director. He/she supports the Executive Sponsor in the strategic oversight and management of a diverse portfolio of work for one or more key accounts. This involves the collection, tracking, and processing of data to inform decision making, managing the day-to-day communication between the sponsor and internal stakeholders, ensuring project budgets and timelines are being managed appropriately, facilitation of internal and sponsor meetings to discuss strategic planning, business development, pipeline updates, share lessons learned, and enhance client service. In particular, the Senior Project Manager will: Be responsible for the overall coordination and management of administrative aspects of individual studies from receipt of lead through project set-up and delivery to the sponsor, including but not limited to financial and legal aspects of project management. Be responsible for financial stewardship and dashboard reporting of the account, per sponsor requirements. Work to ensure that all project deliverables meet the customer time/quality/cost expectations. Work with senior management and functional area leads to identify and evaluate fundamental issues on the project and ensure solutions are implemented. Able to escalate and communicate risks and concerns, as well as develop mitigation plans specific to project needs Oversee and manage diverse real-world evidence projects for multiple stakeholders within a key account; perform traditional project management activities such as ensuring all project deliverables, timelines, and budgets are closely monitored, as well as oversee Quality Control processes, ensure appropriate documentation of quality validation steps, oversee and manage third-party vendors, and keep relevant internal and sponsor stakeholders informed/consulted as appropriate. Contribute to the design and refinement of accounts-specific tools and processes as needed to meet or exceed client expectations with regards to account management. Support client communication, both providing key messaging to internal team members, but also disseminating study team communications to clients and external stakeholders Work across functional groups and departments to ensure successful delivery of studies, including but not limited to data analytics programmers and research scientists. Engage internal teams in discussions to share lessons learned, share ideas for improvement, and discuss strategic approach to Real-World Evidence positioning and business development. Support new sales opportunities including, but not limited to, budget development, proposal content development, and ‘win’ strategies Provide support for the Data Analytics Sr Leadership Team in defining and meeting specific business targets Identify opportunities to expand the account and enhance client service; propose solutions and recommendations both internally and to the sponsor directly. Work on site at client offices 40-60% of work week; regularly meet face-to-face with key client contacts to discuss status of ongoing studies, pipeline, and administrative topics. Qualifications and Experience Bachelor’s degree or licensed certified health care training or equivalent combination of education and experience that provides the individual with the required knowledge, skills and abilities. Project management certification (e.g. PMP, PgMP, CAPM) or demonstration of project management skills including scope, budgeting, forecasting, timelines, resource management, and use of project management systems (e.g. MS Project). Demonstrable experience managing across a range of cross-functional, global, external stakeholders. A demonstrated track record of project managing a variety of studies within ideally either a CRO or consulting firm A deep understanding of the Life Science industry In depth understanding of observational projects and project portfolio management Strong written and verbal communication Proven ability to multitask and problem solve Excellent client facing skills Valid Passport, where appropriate. The position is permanent, full time and optimally based in Bethesda; 40-60% working on-site at sponsor’s office. Company Summary Evidera is a global research consulting group that partners with life sciences organizations worldwide to develop, capture, and communicate the clinical and economic evidence required to substantiate the value of their products and optimize their products’ market access and commercial success. Our research and consulting services are driven by world-class science, operational excellence, and thought leadership and leverage a unique combination of capabilities in health economics, outcomes research, market access, data analytics, and epidemiology. Why Choose Evidera? Evidera offers a competitive salary and benefits package. Our Bethesda office is conveniently located a few blocks from the Bethesda metro, local shops, and restaurants. This office also offers complimentary coffee & tea, breakfast on Fridays, frequent social events, and a spacious, quiet work environment. We are committed to providing training and professional development, with ample opportunity to advance for all our staff. The Real-World Evidence team constitutes a vibrant and dynamic group of individuals who specialize in scientific methods and research operations. Our mission is to be the global leader in generating and communicating evidence of product value to inform healthcare decision making. Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color , religion, sex, national origin, age, genetics, sexual orientation, gender preference disability, or status as a qualified individual with a disability or protected veteran.

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Senior Global Recruiter Human Resources (Waltham, MA or Bethesda, MD)

24 days ago
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Deploy best practices in recruiting, and innovative recruiting techniques best suited to the Evidera candidate pool. Stay informed of relevant industry issues, macro-economic labor markets and ...

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Senior Research Leader – Patient-Centered Research (Bethesda or Seattle)

about 1 month ago
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Senior-Research Leader – Patient-Centered Research – Bethesda or Seattle This position can be based in our Bethesda or Seattle offices. Remote opportunities will also be considered, depending on experience. Position Summary Nationally and/or internationally recognized for health outcomes work with high external visibility and strong track record of publications and presentations. Maintains an established line of PCR research and expertise and provides senior level mentorship and oversight of junior scientific staff. Has broad responsibility for overall financial performance of the PCR organizations and substantial input into business and strategic development. Key Skills and Attri

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Managing Consultant – Market Access Consulting (Waltham, MA)

about 1 month ago
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Managing Consultant– Market Access Consulting– Waltham, MA The Team The complex and rapidly-changing payer environment is becoming increasingly difficult to navigate. Our expert market access teams, comprising industry leaders, former payers, policy experts, and experienced strategists, help clients steer a path through diverse evidence requirements and potential payer barriers to achieve optimal price and access. Dedicated market access teams in London and Waltham, MA, have been providing global payer research and pricing, reimbursement and market access strategy advice to clients in the biopharmaceutical industry for two decades. Our work is underpinned by relationships with high le

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Senior Manager, Real World Evidence - Data Analytics

about 2 months ago
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The Team Evidera has been providing epidemiology, data analytics, and outcomes research services to clients in the biopharmaceutical industry for over 19 years. The Real-World Evidence team supports ...

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Research Associate I - Modeling and Simulation

about 2 months ago
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What you bring to Evidera * Basic understanding of research methods. * Practical knowledge of research project implementation. * Experience working with modeling/simulation software, in particular ...

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