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72 đź’Ľ Science Jobs / Employment in Waltham, MA

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

newabout 11 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 11 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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Director of Scientific Project Management

newabout 15 hours ago
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Director of Scientific Project Management At AstraZeneca, innovation is more than just research. As one of the worlds leading pharmaceutical companies, we’re focused on developing medicines that make a real difference in patient care. This is a place with an entrepreneurial and collaborative culture, where you’ll feel valued, energised and rewarded for your ideas and contributions. A place where talented people can immerse themselves in their work and make significant contributions towards scientific and commercial excellence. We push the boundaries of science to deliver medicines that transform the lives of people around the world. As a Director of Scientific Project Management (oncology) youll be working within one of the strongest science hubs in the world with an incredibly strong early stage portfolio in Waltham Ma. Main Duties and Responsibilities As one of a team of Directors of Scientific Project Management you will be a senior leader working in Early Clinical Oncology. You will use your expertise to partner with the Medical Science Director to enable clinical programme design and be accountable for the operational delivery of programmes of clinical studies which have been designed to establish suitability of compounds for late stage development. As a Director of Scientific Project Management, you will be key player in the work of the product development team(s), working in close partnership with the lead physician for assigned compounds to formulate the clinical development plan. Responsible for managing global or regional scientific projects ensuring project strategy guidelines are adhered to or as an expert involved in the design, conduct and monitoring of clinical oncology projects. Will ensure the clinical projects are delivered within the agreed budgets and in accordance with GCP. Will be responsible for overseeing the development of the functional strategy or act as a renowned expert in own field. Essential Requirements Bachelor of Science degree in a related discipline, preferably in biological science. Significant experience in global drug development and clinical delivery leadership preferably in the Ph1/2 area for oncology programmes. Demonstrate a proven ability to develop clinical programmes to meet business goals and to assess business risk versus potential value, and the ability to align work with global business requirements. Significant experience of clinical programme management and use of project management techniques in complex projects, including resourcing and financial management. Strong strategic influencing skills and the ability to influence broadly within and outside the organisation are important, as is a proven experience of clinical research provider selection/oversight and leading delivery through collaboration with interface organisations and

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Senior Director, Biostatistics

newabout 19 hours ago
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US- MA - Waltham Job ID 2019-1908 # of Openings 1 Category Biometrics - Dept Overview The Senior Director Biostatistics oversee all the biostatistics, data

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Director, Drug Product Technology

newabout 19 hours ago
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US- MA - Waltham | US-PA-Wayne Job ID 2019-1912 # of Openings 1 Category Pharmaceutical Development/Operations Overview Employer is searching for a Director, Drug

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Senior Medical Director, Pharmacovigilance

newabout 19 hours ago
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…skills and mature verbal communication and presentation skills. PM18 PI108356425 Pandologic. Keywords: Medical Director, Location: Waltham , MA - 02451

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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.

Head of Pharmaceutical Science/Development

new1 day ago
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Head of Pharmaceutical Science/Development Head of Pharmaceutical Science/Development Job Locations US-PA-Wayne | US-MA-Waltham Posted Date 4 weeks ago(2/25/2019 8:35 PM) Job ID 2019-1913 of Openings 1 Category Pharmaceutical Sci - Dept Overview Radius Health is searching for a Head of Pharmaceutical Science/Development, Tech Ops. with sound technical and leadership capabilities to develop our promising pipeline and support our commercial products. Reporting to the Senior VP of Technical Operation and a member of the Technical Operations Leadership Team, this role is accountable for leading and developing a high performa

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Sr Product Designer

new1 day ago
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Our client is looking for a Sr Product Designer in Waltham, MA. Who you'll work with Working within the Technology function at our client, they are developing the tools to power the next generation of management consulting. Our client does not accept their esteemed organization's past success, but challenge it, as they utilize design thinking and digital technologies to create new ways of working that will define the future of how they deliver professional services. You will be a core member of the Design Innovation team. You will be part of a global team that is distributed across Boston, New York, New Delhi, and Prague. The Design Innovation team is responsible for using user-centered methods to inform the development and delivery of technology-enabled products and services used across the Firm. This work ensures that they create experiences that make the work of their colleagues faster, easier and more effective. And that they incubate new ways of working that will move the Firm forward. What you'll do You will contribute to all aspects of the product development lifecycle ndash from research and ideation through to detailed design and delivery ndash with an emphasis on rapid prototyping, frequent validation with end users, and creatively approaching constraints. You will collaborate closely with product managers, developers and other disciplines to identify what will be most critical to the success of a product, what it should feel like to interact with a product or service across multiple touchpoints, and to define how theybring that experience into reality. In this work, you will actively look for opportunities to apply new tools and technologies that can help enrich the capabilities the firm provides to our colleagues to do their work. You will also have the opportunity to be an advocate and coach for design thinking, helping others in the firm develop their knowledge, skills, and capabilities in the use of empathetic, inventive and iterative methods for product development. Qualifications middot BS or MS in Interaction Design, Cognitive Science, HCI or equivalent experience middot Minimum 4 years of hands on experience developing digital products across different mediums like web and mobile (familiarity with an Enterprise or agency setting is a plus) middot Ability to design and execute qualitative and quantitative research programs that generate insights to inform the design process middot Ability to create professional-quality, well-designed project deliverables that clearly and persuasively communicate the UXUI design for a product and the reasoning behind it. (e.g. work plans, research protocols, research findings, personas, user flows, wireframes, prototypes and product specs middot Experience creating user interfaces for software products that can be mapped directly to the business and user requirements of the project as well as clearly embody the UX strategy middot Interaction and Visual design skills including user of a diverse set of tools, e.g. Sketch, InVision, Adobe Creative suite, OmniGraffle, etc. middot Strong communication skills with ability to articulate and optimize design based on the value to the user and the business middot Strong ability to collaborate effectively with development teams to ensure that design specifications are implemented, and the usability of products is optimized despite underlying system complexity or constraints middot Experience working with distributed teams middot Ability to thrive in a fluid and entrepreneurial environment and embark on regional and global travel as needed

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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

Scientist, NGS Informatics, Oncology - Senior Scientist Biostatistics - Waltham

new2 days ago
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Kelly Services is currently seeking a Scientist, NGS Informatics, Oncology - Senior Scientist Biostatistics in Waltham, MA to work a contract assignment of 11 months for one of our top clients. Kelly is a full service workforce solutions provider to 98% of the Fortune 100™ companies. We provide employment to more than 700,000 people annually and we deal with some of the largest and best companies both nationally and locally. Primary Responsibilities of the Scientist, NGS Informatics, Oncology - Senior Scientist Biostatistics includes: Mission: As a Scientist, NGS Informatics, Oncology in Waltham, MA, USA or Cambridge, UK you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. IMED (Innovative Medicines and Early Development) focuses on scientific advances in small molecules, oligonucleotides and other emerging technologies and drug discovery platforms across our focus areas. With our vision in Oncology is to help patients by redefining the cancer-treatment paradigm, with the aim of bringing six new cancer medicines to patients between 2013 and 2020. A broad pipeline of next-generation medicines is focused principally on four disease areas - breast, ovarian, lung and hematological cancers. As well as other tumor types, these are being targeted through four key platforms - immunotherapy, the genetic drivers of cancer and resistance, DNA damage repair, and antibody drug conjugates, underpinned by personalized healthcare and biomarker technologies. Main Duties and Responsibilities There is an exciting opportunity for a talented and motivated bioinformatician, eager to bring NGS data together in new ways, to join the group as a Scientist. In this role, you will: Manages, analyses, and deliver customer sequencing data. Develops, tests, and supports data analysis tools and pipelines. Ensure proper movement and automation of data from sequencer to data storage unit. Validate the quality of the datasets using various tools to assess the correctness of the results. Troubleshoot data quality issues by collaborating with Lab and other personnel. Assists with developing requirements for internal software development. Build and maintain high level of experience with team's software and IT technologies. Work collaboratively with scientists and outside collaborators to cultivate, process, and analyse genomic information Develop and maintain an in depth understanding of the scientific and technological domains supported by the NGS Informatics team. Design and apply innovative computational/statistical algorithms and visualizations to: Generate actionable biological insight from genomic data. Build and steer further development of small prototype tools for bench scientists to access and visualize genomic data. Finally, you will collaborate with industry and academia, and exploit external resources, to find the most effective solutions to problems. An enthusiasm to explore non-traditional approaches to bring big data together in biologically meaningful ways. Programming in a Unix and Windows environment. Desirable: A publication track record. Networked within external bioinformatics and NGS communities. An understanding of the contribution of bioinformatics to drug discovery. Effective contributing to collaborative projects involving cross-disciplinary and global teams. Awareness of graph modeling, machine learning, Bayesian analytics or other non-traditional approaches to model biological data. Python/Perl programming expertise. SQL/Database management expertise. Education and Experience Requirement of the Scientist, NGS Informatics, Oncology - Senior Scientist Biostatistics includes : Relevant MS/PHD degree (MS degree with 2 years’ experience desirable) Additional Information: Contract assignment, duration 11 months. Work schedule: full-time, first shift. Kelly Temporary Employee Perks: Group medical, prescription, vision, dental, life, and short-term disability insurance options that are available for purchase—and the coverage is portable Service bonus plan and Holiday pay plan, if qualified Weekly electronic pay options Free online training campus available Exclusive online employee community Corporate discounts Apply Now This position is recruited for by a remote Kelly office, not your local Kelly branch. To be considered for this position you must submit your resume to the Scientific Recruiter listed below: Sandy at: Sanm174KellyServices.com Thank you for your interest in the assignment. Why Kelly ® ? With Kelly, you’ll have access to some of the world’s highest-regarded scientific organizations— providing you with opportunities to work on today’s most challenging, research-intensive, and relevant projects. Our connections can lead you to innovative scientific pursuits you’ll be proud to help advance. We work with 95 of the Fortune 100™ companies, and found opportunities for more than 9,000 scientific professionals last year. You pursued a career in science to fuel your quest for knowledge and your desire to make the world a better place. Let Kelly fuel your career—connect with us today. About Kelly Services ® As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2017 was $5.4 billion. Visit kellyservices.com and connect with us on Facebook , LinkedIn and Twitter . Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is committed to employing a diverse workforce. Equal Employment Opportunity is The Law.

Clinical Trial Manager

new2 days ago
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Radius Health Radius Health is an equal opportunity employer. EEO/Disabled Individuals/Veterans. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to HRconnectradiuspharm.com. Click here to navigate to the “EEO is the Law” poster. Click here to navigate Radius Health’s Pay Transparency Policy. US-MA-Waltham Job ID 2019-1890 of Openings 1 Category Clinical Ops - Dept Overview The Clinical Trial Manager manages and oversees clinical operation activities across a single clinical program or group of related studies, and ensures all assigned operational trial deliverables are met according to timelines, budget, operational procedures, quality standards, SOPs and business guidelines. Responsibilities Contributes to Global clinical / regulatory submissions (FDA, EMA, Canadian and other countries), by helping out with in house and site inspection readiness planning/training, Manages clinical study/studies according to global regulatory requirements. Leads cross functional study execution team to ensure goals and timelines are met. Manages and oversees CRO/Vendors to ensure compliance with processes and regulatory guidelines. Manages MS Project timeline. Supports the tracking of trial budget(s) working closely with the appropriate partners. Accountable for accuracy and timeliness of trial information in all trial databases and tracking systems. Anticipates potential study issues and prepare contingency plans with minimal oversight. Facilitates Clinical Agreements through Clinical and Legal Review. Reviews all study documents for accuracy and quality content. Drafts sample preparation instructions in accordance to Radius standard operating procedures (SOPs) and good clinical practice guidelines (GCPs). Performs onsite co-monitoring, training, or motivational site visits, as needed. Drives traceability procedures for investigational products and coordinates clinical supply planning with cross functional team members. Develops study specific documents such as pharmacy and operational manuals. Reviews and approves, as needed, study documents such as monitoring reports, essential regulatory packages, ICFs, etc. Trains CRO team members and site staff, as needed. Responsible for day-to-day management of vendors working on assigned study, including setting expectations, training, managing timelines and deliverables, and issue management. Provides Clinical Operations input to other important study activities, including but not limited to: site identification and selection, enrollment models, clinical supply planning and drug supply, organization of investigator and vendor meetings, development of informed consents forms, planning and management of Trial Master File, development of monitoring plans, development of systems, development of EDC / Case Report Forms, review of data during the study, data cleaning and database lock, writing the Clinical Study Report. Some travel will be required (10-20% depending on project needs). Qualifications BA/BS in a scientific field (preferred) of study with 5 years of relevant experience working in Clinical Operations in the Pharmaceutical/ biotech industry and/or a CRO. CRA experience preferred. Experience with trial master file organization, regulatory documents, inspection preparation/readiness (site and Sponsor) and all aspects of trial and vendor management. Strong verbal and written communication skills. Ability to deal with competing priorities, detail oriented and creative problem solving ability is essential. Good working knowledge of the international conference on harmonization (ICH) and good clinical practice (GCP) guidelines and other applicable regulatory guidelines required; basic statistical knowledge a plus. Ability to work independently and also in a collaborative team environment. Excellent computer skills (Microsoft Office Suite, Project, Word, Excel, PowerPoint, Outlook; Electronic Data Capture Systems). PI108356524

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Software Quality Assurance Engineer

new2 days ago
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RESPONSIBILITIES Kforce has a fast-growing technology startup client seeking a Software Quality Assurance Engineer in Waltham, Massachusetts (MA). Summary The client is seeking a Software Quality Assurance Engineer to join their team to test both mobile and web technologies at the core of their products. The ideal candidate will be able to achieve a thorough understanding of the client's mobile technology, portals, SAAS application, and back end. The candidate is expected to write test cases based off user stories, create reports, test the app from a design and usability perspective and support both manual and automated testing throughout the lifecycle of the product. The Engineer will be expected to work in a dynamic, interactive team, communicate efficiently and effectively and always be ready to support their peers. The QA Engineer is expected to work closely with the Product team to do exploratory testing around any issues reported by customers, as well as prioritize upcoming features against bugs to ensure the best experience for the customers. Responsibilities Create and maintain test plans for new and existing features Test (mobile and browser based) applications from user standpoint as well as functional testing Review features in development and be able to identify incomplete specifications or prospective testing risks Keep all departments updated on the status of a release and communicate any blockers or delays when testing a release, through reporting and metrics REQUIREMENTS Experience testing on one or more platforms including iOS, Android and web applications Experience working in an Agile environment Experience creating a manual test suite for new products Experience supporting a release from a QA standpoint A passion for breaking things Bonus points if you have healthcare claims experience Kforce is an Equal OpportunityAffirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.

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

new3 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

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Director, HEOR

new4 days ago
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Alkermes, Inc is seeking a Director to join the Health Economics & Outcomes Research (HEOR) team (located in Waltham, MA) to develop and execute strategic plans to support the value proposition of Alkermes products through each stage of the lifecycle. He/she will develop and implement (US) economics and outcomes strategy for one or more products within a therapeutic area. This is a strategic as well as a technical position with project-specific responsibilities. The Director will collaborate with colleagues in other functional areas including those in Clinical Development, Medical Affairs, Government Policy, Regulatory, Brand and Payer Marketing, and National Account Teams. This person must have a successful track record of developing HEOR strategies and executing project plans for products in development through post-launch. This position reports to the Senior Director / Head of HEOR. Key Responsibilities: Support the development of clinical, economic, and patient-centered value propositions related to Alkermes’ products Lead the development of HEOR strategy and supporting tactics for Alkermes’ products.Studies may include, but are not limited to: o Retrospective database analyses o Cost-effectiveness and budget impact models o Indirect treatment comparisons and systematic reviews o Non-interventional real-world effectiveness studies o Clinical outcomes assessment (COA) measure development and validation Effectively lead external research partners to ensure projects are scientifically rigorous, medically relevant and address business needs as well as the needs of patients, health care providers and payers. Support the development of the AMCP and other value dossiers, peer-review publications as well as tools that support formulary decision making and treatment of appropriate populations Collaborate with home office and field-based internal experts in the development and execution of field-based, customer-focused initiatives (e.g., models, dossiers, scientific communications, slide kits, formulary/regulatory dossiers) Train and support internal colleagues (e.g., medical and payer field teams) on HEOR methodologies and data results Provide technical oversight and guidance to research support staff; serve as an internal resource for research design, HEOR methodologies, analytic techniques and reporting of health economic and outcomes research Ensure that Alkermes’ clinical development programs contain outcomes measures that are appropriate and meaningful to patients, health care providers and payers Maintain close working relationships with cross functional colleagues within Medical Affairs, Clinical Development, Regulatory, Marketing, field teams) to support and enhance clinical development programs and access to our products Identify and maintain successful research relationships with HEOR key opinion leaders and other clinical/academic consultants Represent the Alkermes Medical Affairs department for HEOR-related activities at external professional, scientific meetings and forums Desired skills and experience: Advanced degree (PhD, MD, MPH, or PharmD) in a scientific discipline. A clinical background should be supplemented with advanced quantitative training demonstrated by an MPH or MS in a relevant field. Minimum of 7 years of experience in health economics, and outcomes research; with at least 3 years within a pharmaceutical or biotech company In-depth knowledge of the healthcare industry including the pharmaceutical industry (R&D, clinical research and commercialization) as well as the managed care marketplace, hospital systems, and integrated systems of care Competency in medical science, epidemiology, clinical trials, drug development, outcomes research, and pharmacoeconomics including a deep understanding of research methods, health economics, and related disciplines Demonstrated capabilities to develop HEOR strategic plans and manage multiple studies simultaneously; excellent project management to ensure studies delivered on time and within budget Excellent process and project management skills including the ability to manage a significant volume of projects with exercise of good triage and judgment skills Track record of publications in peer-reviewed journals demonstrating experience in COAs, observational research, and/or health economics Results oriented and excellent analytic and collaboration skills combined with robust project management capabilities Proven record of outstanding written and verbal communication and negotiation skills, with experience interacting with and presenting to key customers Ability to manage complexity and ambiguity in a highly matrixed work environment; demonstrated business acumen Highly motivated self-starter who is able to work independently, deal with complex issues, develop creative solutions to complex problems, and relate to multiple internal and external stakeholders Neuroscience/CNS therapeutic experience preferred

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Associate Director/Director – Biologics Downstream Process Development

new4 days ago
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This position is responsible for leading the Biologics Downstream Process Development Team in taking Alkermes’ biologics candidates from discovery through process development, scale-up, optimization, process characterization, tech transfer, clinical production, validation and commercial launch. The Team will also work with external development and manufacturing organizations. The Biologics Process Development labs will be located in Waltham, MA with scale-up capabilities up to 200 L scale. This position will lead a group responsible for: Downstream process development, scale up, and optimization Process Characterization and Control Strategy Development Tech transfer to CMO/CDMOs Support validation and commercial launch Technical support to CMOs for deviations and investigations Qualification of new vendors and CMO/CDMOs Authoring and reviewing technical reports and relevant regulatory submissions Supporting the Regulatory group in responding to agency questions In-depth knowledge in GMP systems, sterile processing, and US/EU requirements Manufacturing tox and clinical supplies Working closely with Biologics Discovery, CMC teams, and Technical Operations to ensure product success Education / Experience Qualified candidates should have a PhD in Engineering with 15 years technical and management experience in biopharmaceutical based process development and GMP manufacturing with an established track record of successfully developing and commercializing biologic products and processes. Skills / Attributes Needed Leadership & Management Strong leadership qualities (integrity, honesty, empathy, confidence, inspiration, commitment, passion, good communicator, decisive, accountable, delegates, empowers, creative/innovative) A collaborative, passionate, empathic personality with excellent interpersonal skills that positively influences the group culture and team dynamics Active participation in team environments and freely offers constructive opinions and suggestions with the expectation they will support their teammates to assure project success Ability to lead and influence technical teams and mentor less experienced scientists and engineers Foster a culture of continuous improvement and operation excellence Detailed understanding of science and engineering principles along with up to date knowledge ofupstream biologics processing technology and regulatory expectations Experience with developing process for novel modalities and non-antibody recombinant protein products expressed in mammalian cell culture Experience in downstream biologics process development, scale-up and optimization along with a strong understanding of analytical technologies that can help enhance process understanding Demonstrated expertise and understanding of downstream unit operations such as chromatography, UF/DF, Depth Filtration, Centrifugation, Nanofiltration and viral clearance steps Experience with pilot scale operations and large scale equipment Energized solving technical problems, learning, creative thinking, and critical analysis and is committed to taking action and getting results Demonstrated knowledge and experience in designing experiments (DOE) and establishing operating ranges as well as establishing control strategies Excellent verbal, writing, and presentation skills with the ability to present concepts and results in a convincing, confident manor and to adjust presentation depth to meet needs of the intended audience

jobs byAdzuna

Associate Director/Director – Biologics Upstream Process Development

new4 days ago
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This position is responsible for leading the Biologics Upstream Process Development Team in taking Alkermes’ biologics candidates from discovery through process development, scale-up, optimization, process characterization, tech transfer, clinical production, validation and commercial launch. The Team will also work with external development and manufacturing organizations. The Biologics Process Development labs will be located in Waltham, MA with scale-up capabilities up to 200 L scale. This position will lead a group responsible for: Support clone selection and cell banking Media and feed development and optimization Upstream process development, scale up, and optimization Process Characterization and Control Strategy Development Tech transfer to CMO/CDMOs Support validation and commercial launch Technical support to CMOs for deviations and investigations Qualification of new vendors and CMO/CDMOs Authoring and reviewing technical reports and relevant regulatory submissions Supporting the Regulatory group in responding to agency questions In-depth knowledge in GMP systems, sterile processing, and US/EU requirements Manufacturing tox and clinical supplies Working closely with Biologics Discovery, CMC teams, and Technical Operations to ensure product success Education / Experience Qualified candidates should have a PhD in Engineering with 15 years technical and management experience in biopharmaceutical based process development and GMP manufacturing with an established track record of successfully developing and commercializing biologic products and processes. Skills / Attributes Needed Leadership & Management Strong leadership qualities (integrity, honesty, empathy, confidence, inspiration, commitment, passion, good communicator, decisive, accountable, delegates, empowers, creative/innovative) A collaborative, passionate, empathic personality with excellent interpersonal skills that positively influences the group culture and team dynamics Active participation in team environments and freely offers constructive opinions and suggestions with the expectation they will support their teammates to assure project success Ability to lead and influence technical teams and mentor less experienced scientists and engineers Foster a culture of continuous improvement and operation excellence Detailed understanding of science and engineering principles along with up to date knowledge ofupstream biologics processing technology and regulatory expectations Experience with developing process for novel modalities and non-antibody recombinant protein products in mammalian cell culture Experience in upstream biologics process development, scale-up and optimization along with a broad understanding of analytical technologies that can help enhance process understanding Energized solving technical problems, learning, creative thinking, and critical analysis and is committed to taking action and getting results Demonstrated knowledge and experience in designing experiments (DOE) and establishing operating ranges as well as establishing control strategies Excellent verbal, writing, and presentation skills with the ability to present concepts and results in a convincing, confident manor and to adjust presentation depth to meet needs of the intended audience

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

new4 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

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Full time SLP Position in North Waltham, MA

4 days ago
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ProCare Therapy is working with a client close to North Waltham, Massachusetts that is looking for ... Master's Degree in Communication Sciences and Disorders * Must be license in MA * Must pass drug ...

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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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Scientist, NGS Informatics, Oncology - Senior Scientist Biostatistics

6 days ago
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Kelly Services is currently seeking a Scientist, NGS Informatics, Oncology - Senior Scientist Biostatistics in Waltham, MA to work a contract assignment of 11 months for one of our top clients. Kelly is a full service workforce solutions provider to 98% of the Fortune 100™ companies. We provide employment to more than 700,000 people annually and we deal with some of the largest and best companies both nationally and locally. Primary Responsibilities of the Scientist, NGS Informatics, Oncology - Senior Scientist Biostatistics includes: Mission: As a Scientist, NGS Informatics, Oncology in Waltham, MA, USA or Cambridge, UK you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. IMED (Innovative Medicines and Early Development) focuses on scientific advances in small molecules, oligonucleotides and other emerging technologies and drug discovery platforms across our focus areas. With our vision in Oncology is to help patients by redefining the cancer-treatment paradigm, with the aim of bringing six new cancer medicines to patients between 2013 and 2020. A broad pipeline of next-generation medicines is focused principally on four disease areas - breast, ovarian, lung and hematological cancers. As well as other tumor types, these are being targeted through four key platforms - immunotherapy, the genetic drivers of cancer and resistance, DNA damage repair, and antibody drug conjugates, underpinned by personalized healthcare and biomarker technologies. Main Duties and Responsibilities There is an exciting opportunity for a talented and motivated bioinformatician, eager to bring NGS data together in new ways, to join the group as a Scientist. In this role, you will: Manages, analyses, and deliver customer sequencing data. Develops, tests, and supports data analysis tools and pipelines. Ensure proper movement and automation of data from sequencer to data storage unit. Validate the quality of the datasets using various tools to assess the correctness of the results. Troubleshoot data quality issues by collaborating with Lab and other personnel. Assists with developing requirements for internal software development. Build and maintain high level of experience with team's software and IT technologies. Work collaboratively with scientists and outside collaborators to cultivate, process, and analyse genomic information Develop and maintain an in depth understanding of the scientific and technological domains supported by the NGS Informatics team. Design and apply innovative computational/statistical algorithms and visualizations to: Generate actionable biological insight from genomic data. Build and steer further development of small prototype tools for bench scientists to access and visualize genomic data. Finally, you will collaborate with industry and academia, and exploit external resources, to find the most effective solutions to problems. An enthusiasm to explore non-traditional approaches to bring big data together in biologically meaningful ways. Programming in a Unix and Windows environment. Desirable: A publication track record. Networked within external bioinformatics and NGS communities. An understanding of the contribution of bioinformatics to drug discovery. Effective contributing to collaborative projects involving cross-disciplinary and global teams. Awareness of graph modeling, machine learning, Bayesian analytics or other non-traditional approaches to model biological data. Python/Perl programming expertise. SQL/Database management expertise. Education and Experience Requirement of the Scientist, NGS Informatics, Oncology - Senior Scientist Biostatistics includes : Relevant MS/PHD degree (MS degree with 2 years’ experience desirable) Additional Information: Contract assignment, duration 11 months. Work schedule: full-time, first shift. Kelly Temporary Employee Perks: Group medical, prescription, vision, dental, life, and short-term disability insurance options that are available for purchase—and the coverage is portable Service bonus plan and Holiday pay plan, if qualified Weekly electronic pay options Free online training campus available Exclusive online employee community Corporate discounts Apply Now This position is recruited for by a remote Kelly office, not your local Kelly branch. To be considered for this position you must submit your resume to the Scientific Recruiter listed below: Sandy at: Sanm174KellyServices.com Thank you for your interest in the assignment. Why Kelly ® ? With Kelly, you’ll have access to some of the world’s highest-regarded scientific organizations— providing you with opportunities to work on today’s most challenging, research-intensive, and relevant projects. Our connections can lead you to innovative scientific pursuits you’ll be proud to help advance. We work with 95 of the Fortune 100™ companies, and found opportunities for more than 9,000 scientific professionals last year. You pursued a career in science to fuel your quest for knowledge and your desire to make the world a better place. Let Kelly fuel your career—connect with us today. About Kelly Services ® As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2017 was $5.4 billion. Visit kellyservices.com and connect with us on Facebook , LinkedIn and Twitter . Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is committed to employing a diverse workforce. Equal Employment Opportunity is The Law.

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Director of Project Management

7 days ago
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US- MA - Waltham Job ID 2019-1925 # of Openings 1 Category Clinical Ops - Dept Overview The Director of Project Management provides project leadership to

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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.

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Vice President, Quality Assurance

16 days ago
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Thousands of companies around the world depend on Rocket to solve their most challenging business problems by helping them run their critical infrastructure, business processes, and data, as well as extending the value of these assets to take advantage of cloud and mobile computing, advanced analytics, and other future innovations. Founded in 1990, Rocket Software is headquartered in Waltham, MA, with 31 offices around the world. We are currently seeking a of Global Quality Assurance & Development Operations at Rocket Software. The primary objective of the role is to ensure that the organization enables highest customer satisfaction by delivering products of the highest quality. The role is a key leadership position reporting to the Products Officer, based out of Rocket’s headquarters in Waltham, Massachusetts, with accountability for defining the strategic direction, and execution of all standardization, quality, and automation initiatives across the entire engineering organization. Responsibilities Lead and manage the globally distributed QA, Release, Program and Project Management teams, ensuring successful product and project delivery in a predictable and high-quality manner Define and implement world-class quality engineering processes spanning the whole software development cycle Drive adoption of standardized tools, processes, best practices to achieve high degree of automation in QA and release deployment Establish, improve, measure and report on dashboard, KPI’s, quality methodology and processes for all of Rocket’s products Build and nurture a highly motivated quality engineering organization. Continuously elevate the skill set of team members and enable them to succeed Work with other key stakeholders to design and execute product wise and plan aligned with overall business goals Required Skills 12\ of Quality Assurance practice/team management experience, with overall 12-15 of experience in the domain Currently in a leadership role managing large global teams, with responsibility for quality and release engineering, preferable for enterprise software products Strong understanding, knowledge and experience with software design and architecture, programming languages, databases, and tools across various disciplines (e.g.; mainframe, distributed, web, etc.), and release management, build engineering and program management. Demonstrated experience in driving large scale adoption of process and tool standardization across the product lifecycle with deep understanding of various tools and technology available for software lifecycle management Demonstrated experience in driving automation and efficiency initiatives Ability to effectively communicate with and lead teams in multiple locations Strong analytical and problem-solving skills Excellent verbal and written communication skills - able to understand and convey complex requirements or technical concepts to technical and non-technical audiences and C-level stakeholders Metrics driven hands-on management style

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Director Major Gifts

17 days ago
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cultivating relationships with both current and past AHA donors who have a proven interest in the mission; qualifying and cultivating prospective donors who are not currently associated with AHA to connect them with our mission; becoming a subject matter expert on the American Heart Association’s restricted fundraising programs; securing donations of $100,000 or more while moving donors to their highest level of commitment and involvement; completing a minimum of 150 face-to-face donor and prospective donor visits each fiscal year developing and managing an individual portfolio of approximately 40 individual donors across the assigned region with the ability to give $100 thousand or more closing between $500 thousand and $1.5 million minimum annually from individual donors through a variety of giving mechanisms including but not limited to outright, stock, family foundation, deferred mechanisms, planned gift mechanisms, etc.; conducting solicitation of 10-15 six and seven figure gifts annually for restricted and unrestricted purposes; collaborating with local fundraising directors on strategies and opportunities to identify, cultivate and solicit major gift prospects to support field events and initiatives. Be a resource and leader in transforming donor and volunteer relationships across field campaigns; creating and leveraging customized strategic events in select markets to cultivate donor relationships; attending and supporting affiliate market activities and social events, Health Strategies events, and other hallmark events that drive the AHA’s overall unrestricted revenue campaign; creating and executing individual strategies for donors and prospects in the portfolio to ensure growth of donor relationships; working with the Mission Advancement Team to secure appropriate project information, including budgets, and creating offers, proposals and asks that will be used to secure gifts; maintaining accurate and timely records of all activities in donor database (BBCRM). Report activity, trends, progress and results to National Team Leader, Major Gifts, association-wide Donor Relations team, or other various internal audiences on a monthly basis; participating in training activities and work with other team members to develop programs and strategies to advance the Major Gifts effort. In this role, you will report to the Major Giving Director Eastern Region for our Mission Advancement team and will be based in our Waltham, MA office. Qualifications If you want to join our mission and be a “Relentless force for a world of longer, healthier lives”, review the preferred skills we are looking for below (Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) experience in securing major gifts or large accounts, preferably supporting large scale research on health and/or community issues; experience working with complex donors or clients representing $100,000 or more in revenue or philanthropy with proven fundraising or sales results at the six-and seven-figure level; experience in identifying and developing major giving and/or engagement opportunities that align with organizational mission, goals and strategies at national and local levels; experience with all areas of cultivation, solicitation and closing sales or fundraising; demonstrated collaborative skills with all levels of staff, prospects, volunteers and donors; demonstrated verbal and written communication skills; willingness to work outside standard office hours as needed, including early morning, evenings and weekends in support of your events; willing to travel within your territory on a daily basis as well as occasional travel to other locations in the affiliate and to our National Center in Dallas, Texas for meetings or training.

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Scientist, NGS Informatics, Oncology - Senior Scientist Biostatistics

20 days ago
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As a Scientist, NGS Informatics, Oncology in Waltham, MA, USA or Cambridge, UK you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients ...

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Senior/Principal Scientist, Chemistry

23 days ago
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The role will suit an individual with a passion for science, strong problem-solving skills, and a ... Waltham, MA - 02451

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Medical and Scientific Affairs Director

23 days ago
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Nova Biomedical is hiring a Medical and Scientific Affairs Director to be based in our Waltham, MA headquarters. This role will leverage your experience in diagnosis and management of diabetic ...

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

23 days ago
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Senior Global Recruiter - Human Resources (Waltham, MA or Bethesda, MD) Position Overview ... Experience in consulting environment with exposure to life sciences and/or the pharmaceutical ...

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VP, Global Marketing Access and Policy

about 1 month ago
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…Reporting to the Chief Commercial Officer and based at the global commercial headquarters in Waltham , MA , the VP of Global Market Access and Policy will serve as

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Associate Director of Quality Audits

3 months ago
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They are a medium sized company located in Waltham Ma, that primarily works on developing products ... Company Description EPM Scientific is a global specialist recruitment company working exclusively ...

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

5 months ago
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We are looking to fill this role in our Waltham, MA or London, UK offices The Team Do you have what ... Design of literature searches/algorithms to be implemented in scientific literature databases (i.e ...

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