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122 đź’Ľ Job Watertown Ma Jobs / Employment

Regional CDL A Truck Drivers - Earn Up to $28/Hour - Watertown

newabout 2 hours ago
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Zenith Global Logistics is now hiring Regional CDL A Truck Drivers in Sharon, MA Zenith Global Logistics specializes in logistics for home furnishings. We currently have immediate openings for experienced drivers based in the Sharon, MA area. If you’re an experienced, safety-oriented driver looking to join a company that truly values its drivers. What We Offer: Earn Up to $28/Hour OR .61 CPM (depending on load) Home EVERY Weekend Paid Weekly 100% of Blue Cross/Blue Shield Healthcare Premiums PAID BY US Subsidized health insurance premiums for spouse/dependents Life Insurance – FREE Disability Insurance - FREE Dental insurance Vision insurance 401K - with company contributions Annual safety bonus - Up to $2,500/Year Paid Time Off Employee Assistance Program Financially strong company Job Description: Operate a Class A vehicle for local and regional deliveries of furniture to business locations. Assist in unloading deliveries to customer. Responsible for required paperwork and the preparation of daily logs via Omnitracs Electronic Logging System. Professionally interact with customer and others at points of delivery and/or pickup. Perform work in accordance with federal, state, and local laws and regulations pertaining to operation of heavy motor vehicles on public roads and highways. Driver Requirements: Must have Class A CDL TWO (2) years tractor trailer driving experience Ability to operate single or combination motor vehicles with a gross vehicle weight in excess of 26,000 pounds Able to physically exert up to 100 pounds of force occasionally, and/or 50 pounds of force frequently, and /or 25 pounds of force constantly to move objects Meet physical demands are for medium to heavy work Call 844-217-7982 or Apply Online Today

Senior Clinical Trial Manager - Watertown

newabout 6 hours ago
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Senior Clinical Trial Manager (11115) – Watertown, MA Watertown, MAJob Summary:The Sr. Clinical Trial Manager will be responsible for independently managing multiple clinical trials of moderate to high complexity. The Sr. CTM will assume many critical activities including the management of internal and external stakeholders, ownership of the clinical trial strategy for execution, serving as a key participant in regulatory discussions and leading a high performing study team towards shared objectives.Major Responsibilities:Manages all clinical aspects of study including:Responsible for selection, qualification, and management of vendors to support clinical trial executionDevelops and manages comprehensive study timelines and metrics and ensures completion of study deliverablesProactively identifies and resolves clinical project issuesProvides study-specific training and leadership to clinical research staff, CRO, CRAs, sites and other contract personnel;Plans, executes, and leads study-specific meetings (e.g., internal core team meetings, investigator meetings, Advisory Committee)Participates in site monitoring visits as appropriateProvides input for the design of the Informed Consent Form(s), CRFs, monitoring conventions, edit checks, etcReviews monitoring reports to ensure quality and resolution of site-related issuesEnsures tracking and review of protocol deviations and assesses impact on study dataUses operational and therapeutic expertise to optimize trial design and execution.Typically works with the Director to design clinical trial protocols consistent with the clinical development plan and develop an ongoing data review plan to ensure appropriate patient recruitmentDevelops relationships with investigators and site staff; critical to be comfortable engaging KOLs in scientific discussionParticipates as Core Team Member and assists the Director, Clinical Operations with management of Program level activities.Qualifications (Education, Experience, Knowledge and Skills):BS/BA in life sciences preferredA minimum of 7 years of direct experience in clinical trial executionExperience managing clinical trials both fully outsourced as well as managed directlyExcellent communication (verbal and written), organizational and problem solving skillsPrior experience developing and managing clinical trial budgetsDemonstrated experience with Oncology studies preferredExperience managing external contract research relationships.ABOUT FORMAFORMA Therapeutics’ scientists are passionate about discovering and developing medicines that will make a difference in oncology and other genetically driven therapeutic areas. The Company’s drug discovery engine drives screening and structure-based approaches across broad families of targets involved in tumor metabolism, epigenetics, protein homeostasis and protein-protein interactions. Leveraging a world class network of academic investigators, clinical experts and corporate partners, FORMA combines deep biological insight and chemistry expertise to rapidly create high quality, innovative drug candidates.FORMA is headquartered in Watertown, MA near the epicenter of the Cambridge Life Sciences cluster, with additional chemistry operations in Branford, CT. www.formatherapeutics.comPlease send resumes to [email protected] and reference job code 11115 in the subject line.No phone calls please. Resumes from third party vendors will not be accepted.SHARE

Clinical Trial Manager - Watertown

newabout 13 hours ago
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Clinical Trial Manager (11114) – Watertown, MA Watertown, MAJob Summary:The Clinical Trial Manager (CTM) will be responsible for managing a broader range of activities on large multi-center studies as well as independent management of clinical trials of easy to moderate complexity. The CTM will assume many critical activities to support the Clinical Operations team to execute on clinical strategies to deliver successful operational outcomes across one or multiple clinical trials.Major Responsibilities:Clinical study team member: works closely with the Sr. Clinical Trial Manager (sCTM) and Director, Clinical Operations and is responsible for coordination and tracking of logistics in support of clinical trials.Responsible for tracking study budgets, including invoice and PO management/reconciliation, month end actuals and accruals in support of the sCTM and Finance.Works closely with sCTM and legal to review and approve clinical trial agreements and site-specific study budgets.Tracks study status, enrollment, regulatory documentation, and site start-up status for assigned clinical projects including review and approval of regulatory package for release of clinical supply.Reviews clinical trial documentation including monitoring visit reports, monitoring plans, communication plans, timelines, etc.Responsible for set-up, maintenance, reconciliation, and archiving of electronic Trial Master Files. Coordinates TMF transfer with CROs.Responsible for maintenance of SharePoint.Interacts with CROs, vendors, investigators, monitors and other external partners to provide information and resolution for specific study requests and issues.Assists sCPM in review of study plans and review and approval of informed consent templates.Responsible for agendas and meeting minutes for clinical study team meetings.Manages logistics and coordinates investigator meetings, CRO kick-off meetings, and vendor meetings along with sCPM and external meeting planners.Responsible for set-up and management of ClinicalTrials.gov.Provides management and oversight for Clinpharm Studies and Investigator Sponsored Studies (ISTs)Qualifications (Education, Experience, Knowledge and Skills):BS/BA in life sciences preferredA minimum of 5 years of direct experience in clinical trial executionExcellent communication (verbal and written), organizational and problem solving skillsPrior experience developing and managing clinical trial budgetsExperience managing external contract research relationships.About FORMAFORMA Therapeutics’ scientists are passionate about discovering and developing medicines that will make a difference in oncology and other genetically driven therapeutic areas. The Company’s drug discovery engine drives screening and structure-based approaches across broad families of targets involved in tumor metabolism, epigenetics, protein homeostasis and protein-protein interactions. Leveraging a world class network of academic investigators, clinical experts and corporate partners, FORMA combines deep biological insight and chemistry expertise to rapidly create high quality, innovative drug candidates.FORMA is headquartered in Watertown, MA near the epicenter of the Cambridge Life Sciences cluster, with additional chemistry operations in Branford, CT. www.formatherapeutics.comPlease send resumes to [email protected] and reference job code 11114 in the subject line.No phone calls please. Resumes from third party vendors will not be accepted.SHARE

Senior Clinical Trial Manager - Watertown

newabout 15 hours ago
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Senior Clinical Trial Manager (11115) – Watertown, MA Watertown, MA Job Summary: The Sr. Clinical Trial Manager will be responsible for independently managing multiple clinical trials of moderate to high complexity. The Sr. CTM will assume many critical activities including the management of internal and external stakeholders, ownership of the clinical trial strategy for execution, serving as a key participant in regulatory discussions and leading a high performing study team towards shared objectives. Major Responsibilities: Manages all clinical aspects of study including: Responsible for selection, qualification, and management of vendors to support clinical trial execution Develops and manages comprehensive study timelines and metrics and ensures completion of study deliverables Proactively identifies and resolves clinical project issues Provides study-specific training and leadership to clinical research staff, CRO, CRAs, sites and other contract personnel; Plans, executes, and leads study-specific meetings (e.g., internal core team meetings, investigator meetings, Advisory Committee) Participates in site monitoring visits as appropriate Provides input for the design of the Informed Consent Form(s), CRFs, monitoring conventions, edit checks, etc Reviews monitoring reports to ensure quality and resolution of site-related issues Ensures tracking and review of protocol deviations and assesses impact on study data Uses operational and therapeutic expertise to optimize trial design and execution. Typically works with the Director to design clinical trial protocols consistent with the clinical development plan and develop an ongoing data review plan to ensure appropriate patient recruitment Develops relationships with investigators and site staff; critical to be comfortable engaging KOLs in scientific discussion Participates as Core Team Member and assists the Director, Clinical Operations with management of Program level activities. Qualifications (Education, Experience, Knowledge and Skills): BS/BA in life sciences preferred A minimum of 7 years of direct experience in clinical trial execution Experience managing clinical trials both fully outsourced as well as managed directly Excellent communication (verbal and written), organizational and problem solving skills Prior experience developing and managing clinical trial budgets Demonstrated experience with Oncology studies preferred Experience managing external contract research relationships. ABOUT FORMA FORMA Therapeutics’ scientists are passionate about discovering and developing medicines that will make a difference in oncology and other genetically driven therapeutic areas. The Company’s drug discovery engine drives screening and structure-based approaches across broad families of targets involved in tumor metabolism, epigenetics, protein homeostasis and protein-protein interactions. Leveraging a world class network of academic investigators, clinical experts and corporate partners, FORMA combines deep biological insight and chemistry expertise to rapidly create high quality, innovative drug candidates. FORMA is headquartered in Watertown, MA near the epicenter of the Cambridge Life Sciences cluster, with additional chemistry operations in Branford, CT. www.formatherapeutics.com Please send resumes to careersformatherapeutics.com and reference job code 11115 in the subject line. No phone calls please. Resumes from third party vendors will not be accepted. SHARE

Route Developer - Sales and Service

newabout 18 hours ago
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Dependable Cleaners is seeking a self-motivated Route Developer to join our close-knit organization. We provide a variety of exceptional garment-based services including dry cleaning, shirt laundry, and tailoring. While previous sales experience is beneficial, we will train the right candidate on nuances of our industry. The Route Developer will be at the forefront of our home valet service by servicing their regular customers and they will grow and develop new customers in their territory. The ideal Route Developer will have an engaging personable demeanor with the ability to take initiative and focus on providing great service. Your professionalism, integrity, and excellent communication skills will be highly valued on our team. This is the right opportunity to take your career to the next level. Full time position available at our Watertown/Newton Corner location. To the right Delivery Route Driver, we offer : Base plus commission salary of $35,000-$50,000 based on route performance Excellent Health and Dental Insurance 401k Company phone, vehicle, and uniform are provided for use on the job Employee Recognition and Incentive Programs Extensive training Employee Discount Potential for growth Duties and Responsibilities for Route Developers Include: Grow your territory with provided leads and by sourcing new clients Transportation and delivery of garments/orders within your territory Build strong relationships with the clients you service to ensure high customer loyalty Assist with production/customer service duties as needed Requirements for Route Developers Include: Professional demeanor and appearance Success minded with a competitive drive Good written and verbal communication skills A valid Massachusetts Driver’s License A safe, incident-free driving record (5 years) Must be able to work in inclement weather, lift up to 30 pounds, and exit and enter a vehicle frequently Previous sales or route service experience is a plus Dependable Cleaners ( www.DependableCleaners.com ), a family owned and operated business since 1944, has served the Boston metro area for 70 years. We have 16 locations in the South Shore, Boston, Brookline and Watertown and we pride ourselves in giving our customers the highest quality in clothing care. We are an award winning dry cleaner, including Best of Boston, Mayor of Boston's Greenovate Award, Best of South Shore Living and over 80 Readers Choice Awards. Dependable Cleaners exercises both green business practices and active community outreach programs. Follow us on Twitter: www.Twitter.com/Dependableclean Follow us on Facebook: www.Facebook.com/DependableCleaners Check us out on YouTube: www.Youtube.com/DependableClean After position is offered, a drug and background check will be required. Knoxville News Sentinel. Keywords: Accounts Payable Technician, Location: Watertown, MA - 02472

jobs byAdzuna

Regional CDL A Truck Drivers - Earn Up to $28/Hour! - Watertown

newabout 20 hours ago
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Zenith Global Logistics is now hiring Regional CDL A Truck Drivers in Sharon, MA! Zenith Global Logistics specializes in logistics for home furnishings. We currently have immediate openings for experienced drivers based in the Sharon, MA area. If you’re an experienced, safety-oriented driver looking to join a company that truly values its drivers. What We Offer:Earn Up to $28/Hour OR .61 CPM (depending on load)Home EVERY Weekend!Paid Weekly!100% of Blue Cross/Blue Shield Healthcare Premiums = PAID BY US!Subsidized health insurance premiums for spouse/dependentsLife Insurance – FREEDisability Insurance - FREEDental insuranceVision insurance401K - with company contributionsAnnual safety bonus - Up to $2,500/Year!Paid Time Off!Employee Assistance ProgramFinancially strong company Job Description:Operate a Class A vehicle for local and regional deliveries of furniture to business locations.Assist in unloading deliveries to customer.Responsible for required paperwork and the preparation of daily logs via Omnitracs Electronic Logging System.Professionally interact with customer and others at points of delivery and/or pickup.Perform work in accordance with federal, state, and local laws and regulations pertaining to operation of heavy motor vehicles on public roads and highways. Driver Requirements:Must have Class A CDLTWO (2) years tractor trailer driving experienceAbility to operate single or combination motor vehicles with a gross vehicle weight in excess of 26,000 poundsAble to physically exert up to 100 pounds of force occasionally, and/or 50 pounds of force frequently, and /or 25 pounds of force constantly to move objectsMeet physical demands are for medium to heavy work Call 844-217-7982 or Apply Online Today!

Regional CDL A Truck Drivers - Top Pay, Great Benefits, Safety Bonus! - Watertown

newabout 23 hours ago
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Zenith Global Logistics is now hiring Regional CDL A Truck Drivers in Sharon, MA! Zenith Global Logistics specializes in logistics for home furnishings. We currently have immediate openings for experienced drivers based in the Sharon, MA area. If you’re an experienced, safety-oriented driver looking to join a company that truly values its drivers. What We Offer: Earn Up to $28/Hour OR .61 CPM (depending on load) Home EVERY Weekend! Paid Weekly! 100% of Blue Cross/Blue Shield Healthcare Premiums = PAID BY US! Subsidized health insurance premiums for spouse/dependents Life Insurance – FREE Disability Insurance - FREE Dental insurance Vision insurance 401K - with company contributions Annual safety bonus - Up to $2,500/Year! Paid Time Off! Employee Assistance Program Financially strong company Job Description: Operate a Class A vehicle for local and regional deliveries of furniture to business locations. Assist in unloading deliveries to customer. Responsible for required paperwork and the preparation of daily logs via Omnitracs Electronic Logging System. Professionally interact with customer and others at points of delivery and/or pickup. Perform work in accordance with federal, state, and local laws and regulations pertaining to operation of heavy motor vehicles on public roads and highways. Driver Requirements: Must have Class A CDL TWO (2) years tractor trailer driving experience Ability to operate single or combination motor vehicles with a gross vehicle weight in excess of 26,000 pounds Able to physically exert up to 100 pounds of force occasionally, and/or 50 pounds of force frequently, and /or 25 pounds of force constantly to move objects Meet physical demands are for medium to heavy work Call 844-217-7982 or Apply Online Today!

Clinical Trial Manager - Watertown

newabout 23 hours ago
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Clinical Trial Manager (11114) – Watertown, MA Watertown, MA Job Summary: The Clinical Trial Manager (CTM) will be responsible for managing a broader range of activities on large multi-center studies as well as independent management of clinical trials of easy to moderate complexity. The CTM will assume many critical activities to support the Clinical Operations team to execute on clinical strategies to deliver successful operational outcomes across one or multiple clinical trials. Major Responsibilities: Clinical study team member: works closely with the Sr. Clinical Trial Manager (sCTM) and Director, Clinical Operations and is responsible for coordination and tracking of logistics in support of clinical trials. Responsible for tracking study budgets, including invoice and PO management/reconciliation, month end actuals and accruals in support of the sCTM and Finance. Works closely with sCTM and legal to review and approve clinical trial agreements and site-specific study budgets. Tracks study status, enrollment, regulatory documentation, and site start-up status for assigned clinical projects including review and approval of regulatory package for release of clinical supply. Reviews clinical trial documentation including monitoring visit reports, monitoring plans, communication plans, timelines, etc. Responsible for set-up, maintenance, reconciliation, and archiving of electronic Trial Master Files. Coordinates TMF transfer with CROs. Responsible for maintenance of SharePoint. Interacts with CROs, vendors, investigators, monitors and other external partners to provide information and resolution for specific study requests and issues. Assists sCPM in review of study plans and review and approval of informed consent templates. Responsible for agendas and meeting minutes for clinical study team meetings. Manages logistics and coordinates investigator meetings, CRO kick-off meetings, and vendor meetings along with sCPM and external meeting planners. Responsible for set-up and management of ClinicalTrials.gov. Provides management and oversight for Clinpharm Studies and Investigator Sponsored Studies (ISTs) Qualifications (Education, Experience, Knowledge and Skills): BS/BA in life sciences preferred A minimum of 5 years of direct experience in clinical trial execution Excellent communication (verbal and written), organizational and problem solving skills Prior experience developing and managing clinical trial budgets Experience managing external contract research relationships. About FORMA FORMA Therapeutics’ scientists are passionate about discovering and developing medicines that will make a difference in oncology and other genetically driven therapeutic areas. The Company’s drug discovery engine drives screening and structure-based approaches across broad families of targets involved in tumor metabolism, epigenetics, protein homeostasis and protein-protein interactions. Leveraging a world class network of academic investigators, clinical experts and corporate partners, FORMA combines deep biological insight and chemistry expertise to rapidly create high quality, innovative drug candidates. FORMA is headquartered in Watertown, MA near the epicenter of the Cambridge Life Sciences cluster, with additional chemistry operations in Branford, CT. www.formatherapeutics.com Please send resumes to careersformatherapeutics.com and reference job code 11114 in the subject line. No phone calls please. Resumes from third party vendors will not be accepted. SHARE

Research Associate/Sr. Research Associate, AD&QC - Watertown

new1 day ago
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We are seeking a flexible, detail oriented analytical thinker as a Research Associate/Sr. Research Associate to join the Analytical Development & Quality Control (AD&QC) team. The successful candidate will work within the internal AD&QC team to develop analytical methodologies for characterization of SQZ Biotechnology's cell therapy products, support internal testing needs, and work collaboratively with Research and Development teams. The successful candidate will also work with external partners to transfer and qualify appropriate test methods. At SQZ, we're proud of our culture and always look to grow our team with people who share our values. We:Squeeze Together: We value teamwork, trust, and transparency as critical components for achieving our mission and exceeding our goals Question Boundaries: We're committed to questioning the status quo and changing the world through our people and our scienceZap Obstacles: We strive to be pioneers. We're resilient when it comes to navigating challenges, anticipated or not, scientific and otherwise Primary responsibilities:Contribute to the development of:Flow cytometry methods to characterize cell therapy products, including elucidation of cell composition for blood products, in-process samples and product materialsCell counting and cell viability methods suitable for deployment in CMC manufacturing settingsAnalytical methods to measure potency of cell therapy productsAnalytical methods for heightened characterization of cellular, donor-based starting materials Conduct studies to understand stability profile of cell therapy productsSupport external method transfer and analytical method qualification activities at contract manufacturing organizations (CMOs)Perform QC activities on materials generated by internal process development team; provide testing support for research and exploratory teams as neededCandidate Must: Independently execute and troubleshoot experiments Manage multiple projects simultaneouslyDiligently document all data in electronic notebooks in a timely mannerCritically analyze and present data Demonstrate critical thinking, problem solving and attention to detailEffectively plan, organize, and schedule work activities to meet deadlinesWork collaboratively in a high-impact team settingMinimum Qualifications:BS or MS in life science or related field (Cell Biology, Biochemistry, Bioengineering, etc.) with at least 1 year of experience in an industry settingExpertise in aseptic techniqueExperience with cell characterization methods and instrumentation (e.g. flow cytometry, FACS, cell counting and viability, hematology analyzers, plate readers)Good understanding of safe lab practices and BSL requirementsExcellent computer skills including experience with Excel, Minitab, GraphPad Prism or similar statistical and data analysis software Preferred Qualifications:Experience with diverse analytical, molecular biology and immunological methods (e.g. U/HPLC, ELISA, ELISpot, Fluorescence and/or Confocal Microscopy, IF/ICS, IHC, FACS, gel electrophoresis, western blot, qPCR)Experience with analytical method qualification and validationsExperience with data processing software like FlowJo, SoftMax Pro, or chromatography analysis softwareExperience writing scientific reports and method SOPs SQZ Biotechnologies is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation or genetics. In addition to federal law requirements, SQZ complies with applicable state and local laws governing nondiscrimination in employment. SQZ does not support relocation for this position.  Life Sciences Job Network. Keywords: Senior Scientist, Location: Watertown, MA - 02472

Regional CDL A Truck Drivers - Top Pay, Great Benefits, Safety Bonus - Watertown

new1 day ago
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Zenith Global Logistics is now hiring Regional CDL A Truck Drivers in Sharon, MA Zenith Global Logistics specializes in logistics for home furnishings. We currently have immediate openings for experienced drivers based in the Sharon, MA area. If you’re an experienced, safety-oriented driver looking to join a company that truly values its drivers. What We Offer: Earn Up to $28/Hour OR .61 CPM (depending on load) Home EVERY Weekend Paid Weekly 100% of Blue Cross/Blue Shield Healthcare Premiums PAID BY US Subsidized health insurance premiums for spouse/dependents Life Insurance – FREE Disability Insurance - FREE Dental insurance Vision insurance 401K - with company contributions Annual safety bonus - Up to $2,500/Year Paid Time Off Employee Assistance Program Financially strong company Job Description: Operate a Class A vehicle for local and regional deliveries of furniture to business locations. Assist in unloading deliveries to customer. Responsible for required paperwork and the preparation of daily logs via Omnitracs Electronic Logging System. Professionally interact with customer and others at points of delivery and/or pickup. Perform work in accordance with federal, state, and local laws and regulations pertaining to operation of heavy motor vehicles on public roads and highways. Driver Requirements: Must have Class A CDL TWO (2) years tractor trailer driving experience Ability to operate single or combination motor vehicles with a gross vehicle weight in excess of 26,000 pounds Able to physically exert up to 100 pounds of force occasionally, and/or 50 pounds of force frequently, and /or 25 pounds of force constantly to move objects Meet physical demands are for medium to heavy work Call 844-217-7982 or Apply Online Today

Security Shift Supervisor Full Time Overnights Watertown, MA - Allied Universal

new1 day ago
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Allied Universal Services is currently searching for a Professional Security Shift Supervisor.Allied Universal is looking for full time security supervisor* Union Site* Restaurants on site. Panera Bread, Casa de Pedro, Branchline, Food trucks every day.* Boston Sports Club and Bright Horizons day care on site (AUS employees get a discount on both)* Shuttle bus services from Back Bay, North Station, and other local areas. Employees can use these services free of charge.* Free campus parking* Valid Driver's License for more than 1 year* Must be comfortable using a computer/tablet* Must be comfortable with access control* $15.71 hourlyThe Shift Security Supervisor will supervise and coordinate the delivery of quality services on a specific shift at an assigned customer. Act as a liaison between site supervisor, Account Manager/Field Operations Manager and professional security officers. Supervise staff on assigned shift, providing coaching, recognition and discipline within approved empowerment range.Supervisory Responsibilities* Communicates staffing needs on shift to Account Manager or Operations Manager* Assures that officers receive appropriate training, developing them in both technical and professional skills; also may include assisting manager in performance management (coaching, counseling, disciplining, performance evaluations, recognition, etc.)* Assures that employee grievances are heard with help from appropriate district or region HR support employees and Account or Operations Manager* Administers JSA's and safety programs outlining site-specific hazards for professional security officers on assigned shift including vehicle / driving safety as appropriate to Corporate procedures* Enforces Allied Universal's policies as outlined in the handbooks and executive memos* Assists with the communication of policies, company announcements and job openings* Provides the basis of a great place to work by treating staff with respectEnforcement of Contract Standards* Helps Account or Operations Manager identify, meet and exceed the needs of the customer* Meets all contractual scheduled hours with a minimum of unbilled overtime* Assists in the coordination and/or conduct site-specific OJT, client specific training and annual refresher training for security personnel* Reconciles security logs against shift responsibilities and patrols; review incident reports prior to submitting to manager and coordinate preliminary investigations* Assists Account or Operations Manager manage uniforms, equipment, supplies and vehicles utilized at the account, maintaining appropriate inventories and maintenance checklistsPhysical and Mental Functions:* Stand or walk constantly (for up to an entire shift) on various surfaces (tile, concrete, carpet)* Climb stairs, ramps, or ladders occasionally during shift* Occasionally bend/twist at waist/knees/neck to perform various duties* Occasionally lift or carry up to 40 pounds* Run as needed* Constant use of both hands and arms in reaching/handling/grasping/fingering while using phone, notepad, writing reports, and other administrative tasks* Constant use of eyes (correctable vision to normal level required) to observe, read, interact with public and co-workers, view security monitors; includes hand/eye coordination* Work in various environments including adverse outdoor conditions such as cold, rain or heat;* Constant mental alertness and attention to detail required while setting priorities and following up on assignmentsQualifications/Requirements:Qualified applicants for the Shift Supervisor position will meet the minimum requirements, as described below:* High school diploma or equivalent required* At least 18 years of age* Must possess effective written and oral communication and interpersonal skills with ability to deal with all levels of personnel and the general public in a professional and effective manner; must be able to use initiative and independent judgment within established guidelines* Must be able to frequently prepare written reports and logs in neat, legible handwriting; may require computer skills* Must be able to read and understand all operating procedures and instructions* Must be able to obtain a valid Guard License as required in the state for which you are applying* As a condition of employment, employee must successfully complete a background investigation and a post-offer/pre-employment drug/alcohol test, may be required to pass Drivers Record check* As a condition of continued employment, employee must maintain current active status of all required License at all times, and must carry the license at all times while on duty* Must display exceptional customer service and communication skills* Remain flexible to ever changing environments; adapt well to different situations* Intermediate computer skills to utilize innovative, wireless technology at client specific sites* Ability to maintain satisfactory attendance and punctuality standard;* Neat and professional appearance* Ability to provide quality customer service* Ability to handle both common and crisis situations at the client site, calmly and efficiently* Read, understand and clearly speak English; constantly use speech and hearing (correctable to normal level required) in communicating with public/co-workers, giving and receiving instructions, using phones* Must be able to handle pressure of working with high volume general public (constantly to occasionally depending on assignment)EOE/Minorities/Females/Vet/DisabilityAllied Universal is an Equal Opportunity Employer committed to hiring a diverse workforce. Allied Universal will provide qualified individuals with reasonable accommodations pursuant to the Americans with Disabilities Act and/or any other applicable state or local laws. We are committed to hiring veterans and reservists. Since 2013, we have hired over 25,000 heroes.#ZR* SAJ* CB-NE

IT Technician - Watertown

new1 day ago
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SQZ Biotechnologies is seeking an IT Technician to join our Operations team reporting directly to the IT Manager. This individual supports the company's employees by troubleshooting, diagnosing, and resolving issues impacting the hardware, software, and services SQZ relies on. The successful candidate will also be responsible for maintenance, upkeep, optimization, and research of software and equipment as needed.At SQZ, we're proud of our culture and always look to grow our team with people who share our values. We:Squeeze Together: We value teamwork, trust, and transparency as critical components for achieving our mission and exceeding our goals Question Boundaries: We're committed to questioning the status quo and changing the world through our people and our scienceZap Obstacles: We strive to be pioneers. We're resilient when it comes to navigating challenges, anticipated or not, scientific and otherwiseKey Responsibilities:Provide support for employees' IT needs on day-to-day basis including helpdesk requests, audiovisual needs, and software troubleshootingInventory and maintain fleet of laptops, tablets, peripherals and other IT assetsProvision new machines and assist with onboarding processesCreate or modify technical operating procedures and process documentationSupporting tasks Windows Server 2016 to manage windows domain including new user set up and group policiesSet up and support workstations/basic audiovisual environmentsCandidate Must:Possess excellent oral and written communication skillsDisplay strong technical and troubleshooting skillsDemonstrate exceptional analytical and problem-solving skillsExhibit strong customer support skillsBe highly organized, detail oriented, and self-motivatedMinimum Qualifications:Bachelor's degree in Information Technology, Computer Science or related field requiredPrior experience with Windows 7 and 10 operating systems requiredPrior experience with Microsoft Office Suite and Google Suites requiredExperience with cloud storage platforms (Box, SharePoint, DropBox, etc.) requiredProficiency with administrating messaging systems and teleconferencing systems preferredKnowledge of Macs and iOS operating system and devices preferredComfort prioritizing and troubleshooting a variety of software and hardware challenges in a fast-paced, start-up environmentCompTIA A , CompTIA Network , and/or Microsoft Server certifications preferredSQZ Biotechnologies is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation or genetics. In addition to federal law requirements, SQZ complies with applicable state and local laws governing nondiscrimination in employment. SQZ does not support relocation for this role.  Life Sciences Job Network. Keywords: IT Technician, Location: Watertown, MA - 02472

Lab Technician - Watertown

new1 day ago
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SQZ Biotechnologies is seeking a Lab Technician, Equipment and Systems to join our Operations team. Reporting directly to the Senior Technician, the successful candidate will directly impact SQZ research by supporting inventory, equipment maintenance and supply chain management. The successful candidate should be highly motivated, takes initiative and can think creatively to solve problems hands-on. This position will be integral for scale up processes for a fast-growing company. At SQZ, we're proud of our culture and always look to grow our team with people who share our values. We:Squeeze Together: We value teamwork, trust, and transparency as critical components for achieving our mission and exceeding our goals Question Boundaries: We're committed to questioning the status quo and changing the world through our people and our scienceZap Obstacles: We strive to be pioneers. We're resilient when it comes to navigating challenges, anticipated or not, scientific and otherwiseKey Responsibilities:Maintenance of laboratory equipment including routine maintenance, troubleshooting, calibration, and interfacing with vendorsProcurement of laboratory consumables and reagents, including communicating with vendors regarding quotes, delivery timelines, and other specific requestsMaintaining inventory and supply chain of lab consumables, including scaling up processes to support company growthMaintenance of SQZ-specific laboratory hardware, including building, cleaning, and maintaining Cellsqueeze devicesCoordination of package receipt with Facilities Technician, including receiving daily packages for laboratory usersInterfacing directly with researchers about supply and equipment needsSupporting process improvement and lab operations as neededCandidate Must:Show technical aptitude for equipment and technical systemsDemonstrate attention to detail and effective organizational skillsDisplay critical thinking and a collaborative attitudeBe comfortable working in controlled environments with hazardous chemicals and gasesManage and prioritize simultaneous projects and deliver consistent resultsPossess effective written and verbal communication skillsMinimum Qualifications:Bachelor's degree or Associate's degree with at least 2 years of industry experience in a laboratory setting requiredExperience troubleshooting laboratory equipment requiredProficient with MS Office Suite (Word, PowerPoint, Excel)Availability to meet the needs of the business that may include early morning, evening, or weekend hoursA strong work ethic, and excitement for being part of an integrated operations teamMust be able to lift up to 25 lbsSQZ Biotechnologies is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation or genetics. In addition to federal law requirements, SQZ complies with applicable state and local laws governing nondiscrimination in employment. SQZ does not support relocation costs for this position. Life Sciences Job Network. Keywords: Laboratory Technician, Location: Watertown, MA - 02472

Research Associate/Sr. Research Associate, Immunology

new2 days ago
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We are looking for a highly motivated, collaborative, and dynamic Research Associate/Sr. Research Associate within our Immunology team within R&D. This role is an opportunity to focus on developing novel immunotherapies for the treatment of cancer and auto-immune diseases. The scope of this work will encompass the design and execution of in vitro and in vivo experiments for internally- and externally-focused research programs. This position requires effective collaboration across multiple groups and the regular presentation of scientific results to multidisciplinary teams.  At SQZ, we're proud of our culture and always look to grow our team with people who share our values. We:Squeeze Together: We value teamwork, trust, and transparency as critical components for achieving our mission and exceeding our goals Question Boundaries: We're committed to questioning the status quo and changing the world through our people and our science¬Zap Obstacles: We strive to be pioneers. We're resilient when it comes to navigating challenges, anticipated or not, scientific and otherwise. Responsibilities:Perform in vivo studies using murine disease models Meticulously execute bench work, analyze data, troubleshoot, and communicate findings Perform in vitro assays using multi-color flow cytometry, ELISA/ELISPOT, and cellular biology methods Deliver biomolecules to cells using the SQZ deviceProcure, organize and maintain inventory of materials needed for experimentsContribute to experimental design and project direction Maintain a lab notebook and contribute to supporting documentation when necessary Contribute to the collective success of the Immunology team Candidate must:Work with skilled teams in a fast-paced, collaborative, and technical research environmentWork independently and manage multiple projects simultaneously Design, execute and troubleshoot experiments Demonstrate critical thinking and problem-solving Demonstrate the ability to critically analyze and present data Effectively plan and organize work activities to meet schedules and deadlines Possess excellent organizational skills and “can-do†attitude Minimum Qualifications:BS/MS in biology, immunology or relevant scientific fieldAt least one year cumulative experience in hypothesis-driven research setting requiredPrior experience with in vivo models strongly preferred, comfort with in vivo models necessaryExpertise in aseptic technique and experience culturing mammalian cells requiredComfort with learning in vivo techniques required. Experience with in vivo techniques preferred Experience with standard immunological assays and familiarity with basic molecular biology techniquesExperience acquiring and analyzing flow cytometry data preferredExperience with GraphPad Prism or similar statistical software preferredSQZ Biotechnologies is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation or genetics. In addition to federal law requirements, SQZ complies with applicable state and local laws governing nondiscrimination in employment. Local candidates only please. Life Sciences Job Network. Keywords: Research Associate, Location: Watertown, MA - 02477

Internal Medicine Physician ( Watertown ) - LocumTenens.com

new2 days ago
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…Call Required: No Board Certification Required: Negotiable Patient Population: Adults Government: No Reference ID: ORD-063285-MD- MA Job Posting ID: 1002173

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Two CRNAs ( Watertown ) - LocumTenens.com

new2 days ago
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…Required: Yes Prescriptive Authority Required: Yes Government: No Additional Information: Anesthesiology Reference ID: ORD-062326-CRNA- MA Job Posting ID: 1001492

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Locum Tenens Emergency Medicine NP Position in Massachusetts ( Watertown )

new2 days ago
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…Call Required: Yes Board Certification Required: Yes Government: No Additional Information: 12,000 -20,000 Reference ID: ORD-063383-NP- MA Job Posting ID: 1003085

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CRNA ( Watertown )

new2 days ago
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…Prescriptive Authority Required: No Government: No Supervision/ Medical Direction (CRNA): Supervision Reference ID: ORD-062601-CRNA- MA Job Posting ID: 999756

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Anesthesiology Locum Tenens Need in Massachusetts ( Watertown )

new2 days ago
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…Per Day: 8 Assignment Duration: Locums Call Required: Yes Board Certification Required: Yes Government: No Reference ID: ORD-063214-MD- MA Job Posting ID: 1001761

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Locum Tenens Addiction Medicine NP ( Watertown )

new2 days ago
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…Required: Yes Prescriptive Authority Required: Yes Patient Population: Adults Support Staff: MA Government: No Reference ID: ORD-063237-NP-NY Job Posting ID:

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Addiction Medicine Physician Assistant ( Watertown ) - LocumTenens.com

new2 days ago
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…No Board Certification Required: Yes Prescriptive Authority Required: Yes Support Staff: MA Government: No Reference ID: ORD-063237-PA-NY Job Posting ID: 1001825

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Sr. Scientist/Scientist, Neurodegeneration - Watertown

new2 days ago
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We are seeking to expand our Exploratory team with a Scientist/Sr. Scientist with a background in Regenerative Medicine. The successful candidate will have a passion for driving high-impact projects focused on the development of novel cell therapies and will be responsible for evaluating SQZ-engineered cells in therapeutic applications. Specifically, this candidate will aid in the design and validation of SQZ-engineered cell therapies utilizing both in vitro assays and in vivo studies to evaluate opportunities in regenerative medicine and neurodegeneration with the goal of advancing the project into clinical development. The qualified individual will have a strong background in Neurodegenerative Disease and Regenerative Medicine.This position requires excellent organizational and interpersonal skills, as the successful candidate will be expected to work productively in a collaborative, cross-functional team environment. Additionally, the successful candidate will contribute to the external scientific visibility of the company through collaboration with large pharmaceutical companies and serve as a subject matter expert in Regenerative Medicine.At SQZ, we're proud of our culture and always look to grow our team with people who share our values. We:Squeeze Together: We value teamwork, trust, and transparency as critical components for achieving our mission and exceeding our goalsQuestion Boundaries: We're committed to questioning the status quo and changing the world through our people and our scienceZap Obstacles: We strive to be pioneers. We're resilient when it comes to navigating challenges, anticipated or not, scientific and otherwiseResponsibilities:Design, plan, and execute complex ex vivo and in vivo assays to evaluate therapeutic efficacy of human and murine engineered cells for the treatment of degenerative and neurodegenerative diseaseServe as a subject matter expert for the use of cell therapies in regenerative medicineMentor research associates and junior scientists Document work in notebooks and technical reportsPrepare presentations for internal and external meetings Participate in an interactive, team-oriented culture, interfacing primarily with a variety of project teamsCandidate Must:Demonstrate excellent oral and written communication skillsPossess the ability to contribute effectively in a cross-functional roleWork independently and as part of a team consisting of a diverse group of science and engineering professionalsWork well within a fast-paced, dynamic, and team-oriented start-up environmentPossess excellent organizational, interpersonal and problem-solving skillsQualifications:PhD in neuroscience, immunology, cell biology, molecular biology, or related discipline is required. Experience with regenerative medicine, neurodegenerative disease, stem cell biology, or iPSCs is essential.Minimum of 2 years experience required. Industry experience is preferred.Strong background in ex vivo primary cell culture and prior experience with human and murine primary cellsExperience with transfection techniques such as electroporation, lipofection, and or viral transduction recommendedHands-on experience with genome editing tools such as CRISPR/Cas9 or transient gene knockdown technologies such as RNAi is required.Prior experience with design of flow cytometry (FACS) panels and ability to perform analysis on both human and murine cells is a plus.SQZ Biotechnologies is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation or genetics. In addition to federal law requirements, SQZ complies with applicable state and local laws governing nondiscrimination in employment. Life Sciences Job Network. Keywords: Senior Scientist, Location: Watertown, MA - 02472

Sr. Scientist/Principal Scientist, Cancer Immunology

new2 days ago
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We are seeking to expand our Exploratory team with a Sr. Scientist/Principal Scientist with a background in cancer immunology. The successful candidate will have a passion for driving high-impact projects developing novel immune-therapies for oncology. The scientist will be responsible for evaluating SQZ-engineered immune cells in immuno-oncology applications. Specifically, this candidate will design and execute complex in vivo and ex vivo tumor studies with SQZ-engineered immune cells and test rational combinations of cancer therapeutics with the goal of advancing the project into clinical development. The qualified individual will have a strong background in tumor biology, immunology, oncology, and/or immuno-oncology.This position requires excellent organizational and interpersonal skills, as this candidate will be expected to work productively in a collaborative, cross-functional team environment. Additionally, the successful candidate will contribute to the external scientific visibility of the company through collaboration with large pharmaceutical companies and serve as a subject matter expert in immuno-oncology.At SQZ, we're proud of our culture and always look to grow our team with people who share our values. We:Squeeze Together: We value teamwork, trust, and transparency as critical components for achieving our mission and exceeding our goalsQuestion Boundaries: We're committed to questioning the status quo and changing the world through our people and our scienceZap Obstacles: We strive to be pioneers. We're resilient when it comes to navigating challenges, anticipated or not, scientific and otherwiseResponsibilities:Design, plan, and execute complex in vivo and ex vivo assays to evaluate anti-tumor efficacy in mice Develop novel murine tumor models to investigate SQZ immunotherapies with the goal of advancing projects into clinical developmentManage/lead therapeutically focused external collaborationsDesign flow cytometry (FACS) panels and perform analysis on murine cells, tumors, and tissuesMentor scientists and research associates Document work in notebooks and technical reportsManage and support external collaborations as a subject matter expert in immuno-oncology Prepare presentations for internal and external meetings Participate in an interactive, team-oriented culture, interfacing primarily with a variety of project teams. Candidate Must: Excellent oral and written communication skillsAbility to contribute effectively in a cross-functional roleDemonstrate ability to work independently and as part of a team consisting of a diverse group of science and engineering professionalsWork well within a fast-paced, dynamic, and team-oriented start-up environmentPossess excellent organizational, interpersonal and problem solving skillsQualifications:PhD in immunology, cancer biology, or related discipline is required. Minimum of 3 years post-doctoral experience with at least 2 years industry experience requiredAbility to independently design and perform in vivo anti-tumor efficacy studies (including tumor implantation and tumor monitoring) Strong background in ex vivo primary cell culture and engineering is recommended. Skilled in ex vivo and in vitro assays involving complex immune cell culture systems, flow cytometry, ELISA, ELISPOT, and intracellular cytokine staining SQZ Biotechnologies is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation or genetics. In addition to federal law requirements, SQZ complies with applicable state and local laws governing nondiscrimination in employment.Life Sciences Job Network. Keywords: Senior Scientist, Location: Watertown, MA - 02477

Engineer

new2 days ago
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SQZ Biotechnologies is seeking an Engineer to join our Process Development and Manufacturing team reporting directly to Senior Manager. The successful candidate will support process development efforts for novel cell therapy products as part of a team of engineers and scientists. He/she will also support manufacturing as the company prepares for technology transfers at different CMOs and cGMP production of a clinical product. This position requires hands-on laboratory work, data analysis, development and maintenance of technical documents, and collaboration across multiple teams and external vendors.At SQZ, we're proud of our culture and always look to grow our team with people who share our values. We:Squeeze Together: We value teamwork, trust, and transparency as critical components for achieving our mission and exceeding our goals Question Boundaries: We're committed to questioning the status quo and changing the world through our people and our scienceZap Obstacles: We strive to be pioneers. We're resilient when it comes to navigating challenges, anticipated or not, scientific and otherwiseKey Responsibilities:Assist the Process Development and Manufacturing team in preparing novel cell therapy products for GMP production and clinical applicationsSupport the development of SQZ Biotech's platform technologyOrganize and develop plans for independent and team-oriented laboratory experiments and associated laboratory analysisCollaborate across different functional teams to ensure successful completion of necessary studiesSupport tech transfer activities of developed process to different CMOsSupport supply chain development to enable successful processing and manufacture of final drug productEstablish and maintain communication with vendors and assist with product procurement, testing, and evaluationDevelop and maintain detailed technical documentation, including plans, reports, and notebook entriesMinimum Qualifications:BS/MS in engineering discipline with focus on biology or chemistryOne-year cumulative experience in a biological laboratory settingStrong communication (oral and written) and interpersonal skillsStrong organizational skills and the ability to successfully manage multiple technical projects and priorities at the same timeProficient with Microsoft Office ToolsSQZ Biotechnologies is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation or genetics. In addition to federal law requirements, SQZ complies with applicable state and local laws governing nondiscrimination in employment. SQZ does not support relocation for this role.  Life Sciences Job Network. Keywords: Biotechnological Engineer, Location: Watertown, MA - 02472

Senior Clinical Trial Manager

new2 days ago
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Senior Clinical Trial Manager (11115) – Watertown, MA Watertown, MA Job Summary: The Sr. Clinical Trial Manager will be responsible for independently managing multiple clinical trials of moderate to high complexity. The Sr. CTM will assume many critical activities including the management of internal and external stakeholders, ownership of the clinical trial strategy for execution, serving as a key participant in regulatory discussions and leading a high performing study team towards shared objectives. Major Responsibilities: Manages all clinical aspects of study including: Responsible for selection, qualification, and management of vendors to support clinical trial execution Develops and manages comprehensive study timelines and metrics and ensures completion of study deliverables Proactively identifies and resolves clinical project issues Provides study-specific training and leadership to clinical research staff, CRO, CRAs, sites and other contract personnel; Plans, executes, and leads study-specific meetings (e.g., internal core team meetings, investigator meetings, Advisory Committee) Participates in site monitoring visits as appropriate Provides input for the design of the Informed Consent Form(s), CRFs, monitoring conventions, edit checks, etc Reviews monitoring reports to ensure quality and resolution of site-related issues Ensures tracking and review of protocol deviations and assesses impact on study data Uses operational and therapeutic expertise to optimize trial design and execution. Typically works with the Director to design clinical trial protocols consistent with the clinical development plan and develop an ongoing data review plan to ensure appropriate patient recruitment Develops relationships with investigators and site staff; critical to be comfortable engaging KOLs in scientific discussion Participates as Core Team Member and assists the Director, Clinical Operations with management of Program level activities. Qualifications (Education, Experience, Knowledge and Skills): BS/BA in life sciences preferred A minimum of 7 years of direct experience in clinical trial execution Experience managing clinical trials both fully outsourced as well as managed directly Excellent communication (verbal and written), organizational and problem solving skills Prior experience developing and managing clinical trial budgets Demonstrated experience with Oncology studies preferred Experience managing external contract research relationships. ABOUT FORMA FORMA Therapeutics’ scientists are passionate about discovering and developing medicines that will make a difference in oncology and other genetically driven therapeutic areas. The Company’s drug discovery engine drives screening and structure-based approaches across broad families of targets involved in tumor metabolism, epigenetics, protein homeostasis and protein-protein interactions. Leveraging a world class network of academic investigators, clinical experts and corporate partners, FORMA combines deep biological insight and chemistry expertise to rapidly create high quality, innovative drug candidates. FORMA is headquartered in Watertown, MA near the epicenter of the Cambridge Life Sciences cluster, with additional chemistry operations in Branford, CT. www.formatherapeutics.com Please send resumes to careersformatherapeutics.com and reference job code 11115 in the subject line. No phone calls please. Resumes from third party vendors will not be accepted. SHARE

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Clinical Trial Manager

new2 days ago
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Clinical Trial Manager (11114) – Watertown, MA Watertown, MA Job Summary: The Clinical Trial Manager (CTM) will be responsible for managing a broader range of activities on large multi-center studies as well as independent management of clinical trials of easy to moderate complexity. The CTM will assume many critical activities to support the Clinical Operations team to execute on clinical strategies to deliver successful operational outcomes across one or multiple clinical trials. Major Responsibilities: Clinical study team member: works closely with the Sr. Clinical Trial Manager (sCTM) and Director, Clinical Operations and is responsible for coordination and tracking of logistics in support of clinical trials. Responsible for tracking study budgets, including invoice and PO management/reconciliation, month end actuals and accruals in support of the sCTM and Finance. Works closely with sCTM and legal to review and approve clinical trial agreements and site-specific study budgets. Tracks study status, enrollment, regulatory documentation, and site start-up status for assigned clinical projects including review and approval of regulatory package for release of clinical supply. Reviews clinical trial documentation including monitoring visit reports, monitoring plans, communication plans, timelines, etc. Responsible for set-up, maintenance, reconciliation, and archiving of electronic Trial Master Files. Coordinates TMF transfer with CROs. Responsible for maintenance of SharePoint. Interacts with CROs, vendors, investigators, monitors and other external partners to provide information and resolution for specific study requests and issues. Assists sCPM in review of study plans and review and approval of informed consent templates. Responsible for agendas and meeting minutes for clinical study team meetings. Manages logistics and coordinates investigator meetings, CRO kick-off meetings, and vendor meetings along with sCPM and external meeting planners. Responsible for set-up and management of ClinicalTrials.gov. Provides management and oversight for Clinpharm Studies and Investigator Sponsored Studies (ISTs) Qualifications (Education, Experience, Knowledge and Skills): BS/BA in life sciences preferred A minimum of 5 years of direct experience in clinical trial execution Excellent communication (verbal and written), organizational and problem solving skills Prior experience developing and managing clinical trial budgets Experience managing external contract research relationships. About FORMA FORMA Therapeutics’ scientists are passionate about discovering and developing medicines that will make a difference in oncology and other genetically driven therapeutic areas. The Company’s drug discovery engine drives screening and structure-based approaches across broad families of targets involved in tumor metabolism, epigenetics, protein homeostasis and protein-protein interactions. Leveraging a world class network of academic investigators, clinical experts and corporate partners, FORMA combines deep biological insight and chemistry expertise to rapidly create high quality, innovative drug candidates. FORMA is headquartered in Watertown, MA near the epicenter of the Cambridge Life Sciences cluster, with additional chemistry operations in Branford, CT. www.formatherapeutics.com Please send resumes to careersformatherapeutics.com and reference job code 11114 in the subject line. No phone calls please. Resumes from third party vendors will not be accepted. SHARE

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Vice President, Legal - Watertown

new3 days ago
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SQZ Biotechnologies is seeking a Vice President/Head of Legal to join our team. This is a newly created role reporting directly to the Chief Executive Officer. As the leader of the Legal function, you will be responsible for advising the SQZ leadership team and contributing to strategic decision making on a variety of matters ranging from investor relations, finance, clinical, human resources, contracts, and facilities. The successful candidate will be a strong business partner with a proven ability to collaborate across all functions. At SQZ we look for individuals that our driven by our mission to empower cells to change lives and share our values: We: Squeeze Together: We value teamwork, trust, and transparency as critical components for achieving our mission and exceeding our goals Question Boundaries: We're committed to questioning the status quo and changing the world through our people and our scienceZap Obstacles: We strive to be pioneers. We're resilient when it comes to navigating challenges, anticipated or not, scientific and otherwise Key Responsibilities:  Oversees all legal matters including investor relations, corporate structures, finance, clinical, human resources, contracts, facilities, and intellectual propertyDevelops functional plans for managing legal matters, including activities to be performed in-house or through third-party relationships Provide counsel on corporate governance related matters and corporate structure Structure, draft, negotiate and advise upon general business transactions to include contracts ranging from routine supply and service contracts to one-off, complex, high-dollar-value transactions Develop, revise, update and maintain the master service, non-disclosure, and other standard form agreements; perform regular internal reviews of existing legacy contracts and ensuring legal and policy compliance Provide counsel to the executive team on a range of compliance, risk management and corporate governance matters Review employment agreements, employment-related documents and assist with employment legal matters as needed  Work closely with CEO and senior team to develop board materials and facilitate approval and governance processes Minimum Qualifications: J.D. degree from an accredited law school and at least 10 years relevant work experience Valid Bar Admission to Massachusetts State Bar At least 5 years prior in-house experience at a life science or biotechnology company required; Startup experience highly preferred Experience leading compliance and corporate governance functions in a public company setting Experience with commercial contract terms and conditions with particular emphasis on the protection of intellectual property, confidentiality and minimizing liabilities and risks Ability to prioritize and undertake mission critical tasks, providing exceptional service to various stakeholders Self-starter who understands executing with urgency Accuracy and attention to detail Excellent interpersonal, written and oral communication skills, as well as a team player attitude; experience with cross-cultural communication a plus Flexible, able to adapt to changes and different challenges in a fast-paced, start-up environment. Experience leading and mentoring teams Excellent and proactive communicator SQZ Biotechnologies is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation or genetics. In addition to federal law requirements, SQZ complies with applicable state and local laws governing nondiscrimination in employment. Life Sciences Job Network. Keywords: Vice President of Legal Affairs, Location: Watertown, MA - 02477

Associate Director, SEC Reporting & Compliance

new3 days ago
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SQZ Biotechnologies is seeking an Associate Director, SEC Reporting & Compliance to join our Finance and Accounting team reporting directly to the head of Finance. This role will be involved in all SEC financial filings, will be responsible for establishing the Company's Sarbanes-Oxley compliance program, will assist in technical accounting support the implementation, maintenance, and review of internal controls and participate in other ad-hoc projects, as needed. At SQZ, we're proud of our culture and always look to grow our team with people who share our values. We:Squeeze Together: We value teamwork, trust, and transparency as critical components for achieving our mission and exceeding our goalsQuestion Boundaries: We're committed to questioning the status quo and changing the world through our people and our scienceZap Obstacles: We strive to be pioneers. We're resilient when it comes to navigating challenges, anticipated or not, scientific and otherwiseKey Responsibilities:Financial ReportingResponsible for preparing the company to meet public company reporting and disclosure requirements and ultimately the preparation of financial reports filed with the SEC including, Forms 10-Q, 10-K and quarterly earnings releases and related XBRL requirementsResponsible for the preparation of the quarterly financial statements including the balance sheet and statements of operations, shareholders' equity and cash flow in accordance with US GAAP, including commentary for the MD&A analysisResponsible for continued compliance with US GAAPContinuously review and monitoring of new accounting pronouncements and competitor's filings to ensure our disclosures are in line with accounting standards and our peer groupWork with the team to support annual audits and quarterly reviewsInternal Controls Lead the development and implementation of internal controls and preparation of SOX 404 complianceOffer recommendations for business process improvementsTechnical Accounting Research and monitor new accounting pronouncements and ensure proper disclosureAnalyze financial, accounting and operational impacts of proposed transactions as requiredAnalyze and develop accounting policies for day-to-day business activities (e.g. new contracts, etc.)Conducts, supports and assists with the initial implementation and ongoing SOX compliance requirementsSupport tax return preparation and other tax requirements Minimum Qualifications:BA/BS in Accounting or Finance, CPA requiredAt least 7 years of relevant accounting experience required, with life science/biotech experience strongly preferredAdvanced understanding of generally accepted accounting principles and the ability to apply GAAP to new and existing transactionsMust have prior SEC reporting responsibilities and clear proficiency in SEC reporting requirements and researchBig 4 experience preferredExperience with ERP system implementationStrong project management, planning, and organization skills, including the ability to handle multiple projects simultaneously in a fast-paced environmentContinuous improvement attitude; ability to independently seek out and implement internal or external best practicesExcellent verbal and written communication skillsStrong team player Attentive to detail SQZ Biotechnologies is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation or genetics. In addition to federal law requirements, SQZ complies with applicable state and local laws governing nondiscrimination in employment. Life Sciences Job Network. Keywords: Finance Director, Location: Watertown, MA - 02472

Associate Director/Director, Translational Medicine - Watertown

new3 days ago
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SQZ Biotechnologies is seeking an Associate Director/Director, Translational Medicine to join our Clinical & Regulatory team reporting directly to the Chief Medical Officer. The Associate Director/Director will be responsible for strategic planning and execution of SQZ's clinical-translational and diagnostic efforts related to the development of cell therapies. The successful candidate will lead the development, documentation, and execution of our immuno-oncology programs. He or she will work in cross-functional teams to assure the highest standards of clinical drug development and GCP.At SQZ, we're proud of our culture and always look to grow our team with people who share our values. We:Squeeze Together: We value teamwork, trust, and transparency as critical components for achieving our mission and exceeding our goalsQuestion Boundaries: We're committed to questioning the status quo and changing the world through our people and our scienceZap Obstacles: We strive to be pioneers. We're resilient when it comes to navigating challenges, anticipated or not, scientific and otherwiseObjectives:Responsible for immunological, genomic and other biomarker aspects of regulatory or communications documents including publicationsResponsible for review of immunological, genomic and other biomarker data of clinical trials Responsible for development, implementation and execution of immunological, genomic and other clinical-translational strategiesResponsible for external data collection and review of competitive intelligenceAccountabilities:Identification and definition of clinical-translational and diagnostic development opportunitiesRecommendation of a translational and diagnostic strategyPharmacodynamic approaches to optimize drug therapyReview of translational like immunological, genomic and other biomarker data Pharmacogenomic/pharmacodynamic support of safety data review for signal detectionAuthor of regulatory or communication documents or sections related to translational medicine or diagnostic and pharmacogenomic strategiesMonitoring of competitor activities and dataResponsibilities include, but are not limited to:Implementation and execution of translational, diagnostic and pharmacogenomic strategyProvide specific translational, diagnostic and pharmacogenomic expertise to enhance innovation and efficiency in clinical developmentTranslational, diagnostic and pharmacogenomic support of Strategic or Clinical Advisory BoardsMonitoring, coding and data cleaning of translational, genomic, diagnostic and pharmacogenomic data together with Clinical OperationsMedical writing of translational, genomic, diagnostic and pharmacogenomic sections in regulatory documents not limited to IND submission, IND annual updates, briefing documents, study protocols, investigator brochures and other study-relevant documents like patient informed consent documentsTimely reporting of translational, genomic, diagnostic and pharmacogenomic data from clinical trials that meet the standards of excellence for ethics, scientific merit, and regulatory complianceInput in research activities related to translational medicineManuscript writing of publications or other documents intended for external audiences related to translational, genomic, diagnostic and pharmacogenomic aspectsSelection of vendors for translational, genomic, diagnostic and pharmacogenomic collaborators and supervision of external collaborators and consultants if applicable Function as the internal resource for all functions requiring translational, genomic, diagnostic and pharmacogenomic input Be the primary point of contact for clinical trial staff at study sites for translational, genomic, diagnostic and pharmacogenomic issuesSupport of safety charters, DMC charters, or other specific management plans or manuals in a cross-functional team if not primary authorSupport or preparation of translational, genomic, diagnostic and pharmacogenomic data interpretation and clinical trial reports Contribute in an active and ongoing manner to the scientific, clinical and commercial development of current and future product candidatesMedical Affairs activities as neededMinimum Qualifications:Medical and/or Doctoral degree and post-doctoral training in a field related to Clinical Pharmacology, Translational Medicine, Pharmacology, Pharmacogenomics or Biomarker ResearchAt least 7 years of experience in academic, biotech or pharmaceutical setting and experience in translational medicine or biomarker developmentStrong interpersonal, organization, planning and communication (oral and written) skills.Extensive knowledge of clinical development, FDA and international global clinical trial regulations and ICH GCP guidelinesExperience with development of cell and gene therapy products, immuno-oncology therapies and development requirements preferredExperience in biomarker and/or genomic-related research in the pharmaceutical/biotech settingMust possess an entrepreneurial and hands-on attitude; and be highly self-motivatedSQZ Biotechnologies is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation or genetics. In addition to federal law requirements, SQZ complies with applicable state and local laws governing nondiscrimination in employment. Life Sciences Job Network. Keywords: Translational Development Manager, Location: Watertown, MA - 02472

Physician / Internal Medicine / New York / Locum or Permanent / Internal Medicine - Internal Medicine Opportunity in Watertown, NY Job

new3 days ago
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North Country Family Health Center - Watertown Full TimeHours: Clinic Hours Monday - Friday 8 AM - 6 PM | 4 Day Work Week Available Employed MD/DO New Graduates Average Patients seen: 8 Hour Day: 19 | 10 Hour Day: 24 Call Schedule: No Call Loan Repayment Sign-On Bonus: $50000 Compensation: $225,000 | 2% Merit Increase Potential | $50K Sign-on Bonus | Potential Loan Repayment Through the NHSC - $75K Loan Repayment for Physicians Who Obtain a Suboxone Waivered License Benefits: - Medical | Dental | Vision - Short and Long Term Disability - Voluntary Life and AD&D - Optional Supplementary Insurance - 403b Retirement Plan Available With up to $2,500 Annual Employer Match - Life Insurance - 4 Weeks PTO With 1 Additional Vacation Day Earned Each Year Worked - Accrual Rate of 1 Sick Day Per Month Up to 630 Hours - Paid Malpractice Insurance - Reimbursement for DEA, Licensure, and One Membership Fee - $2,100 CME Allowance Plus 3 Days Additional Info: - BE physicians accepted and must become BC. - DEA-X a plus - We offer primary medical care plus integrated behavioral healthcare and care coordination services for all ages. - Behavioral health/counseling services, dental care, and WIC on site. - You will be joining a family medicine physician, a pediatrician, 3 nurse practitioners, a psychologist, 2 social workers, 2 dentists, and 3 dental hygienists. - Patient-Centered Medical Home. - Care Coordination and enabling support staff all on site. - Scribing is available for interested providers; all providers have a 2:1 LPN/MA to provider ratio. - No administrative duties required. - Practice went through a workflow improvement program in January 2019 to improve provider satisfaction and work-life balance. - EMR: Centricity - Watertown is a small city in a rural area with big-city conveniences. - Our community boasts a low cost of living, excellent schools, and a safe environment.

Administrative Assistant Boston - Watertown

12 days ago
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Assists and supports the Senior Property Manager 16 hours per week at a property in Watertown, MA and 24 hours at a scattered-site property in Boston. Both properties are comprised of a mixed ...

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Registered Nurse

12 days ago
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The Clinic Nurse provides a variety of direct patient care services including planning, implementing and evaluating direct patient care, assisting with diagnostic and therapeutic procedures, supervising appropriate recording and retention of all medical records, patient education and communication, and administering medications. Graduate from an approved registered or practical nurse program. Current licensure, by the State Board of Nursing, as a Registered Nurse or Licensed Practical Nurse. Minimum two years experience working in a healthcare setting, required. Clinic experience working as a MA, LPN or RN, preferred. CPR certification. Job: Nursing Organization: Watertown Regional Medical Center Title: RN-Cardiology Clinic (FTE 1.0 DAY) Location: Wisconsin-Watertown Requisition ID: 7471-1123

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Senior Clinical Trial Manager

17 days ago
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Senior Clinical Trial Manager (11115) - Watertown, MA Watertown, MA Job Summary: The Sr. Clinical Trial Manager will be responsible for independently managing multiple clinical trials of moderate to ...

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Clinical Trial Manager

17 days ago
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Clinical Trial Manager (11114) - Watertown, MA Watertown, MA Job Summary: The Clinical Trial Manager (CTM) will be responsible for managing a broader range of activities on large multi-center studies ...

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Registered Nurse

19 days ago
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The Clinic Nurse provides a variety of direct patient care services including planning, implementing and evaluating direct patient care, assisting with diagnostic and therapeutic procedures, supervising appropriate recording and retention of all medical records, patient education and communication, and administering medications. Graduate from an approved registered or practical nurse program. Current licensure, by the State Board of Nursing, as a Registered Nurse or Licensed Practical Nurse. Minimum two years experience working in a healthcare setting, required. Clinic experience working as a MA, LPN or RN, preferred. CPR certification. Job: Nursing Organization: Watertown Physician Pract B Title: Clinic RN (FTE 1.0 DAY) Location: Wisconsin-Watertown Requisition ID: 7471-1203

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Physician / Pediatrics / New York / Locum or Permanent / Pediatrics - Pediatrics Opportunity in Watertown, NY Job

about 1 month ago
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Family Practice - Watertown Full TimeHours: 8 or 10 Hour Shifts 5 or 4 Days per week Employed MD/DO New Graduates Average Patients seen: 8 Hour Day: 19 | 10 Hour Day: 24 Call Schedule: Hospital Call Loan Repayment Sign-On Bonus Compensation: Up to $208K | Relocation Assistance under $10K | Sign-on Bonus Under $10K | Potential Loan Repayment Through the NHSC Benefits: - Life Insurance - Retirement with Match up to 50% of 6% Contribution, to a Max of $2,500 Annually - 4 Weeks Paid Vacation, 12 Sick Days and 4 Paid CME Days - $2,100 CME Reimbursement Additional Info: - Hospital rounding including the newborn nursery. - An integrated pediatric site with behavioral health, dental, and WIC program all in the same location. - Patient-Centered Medical Home. - Care Coordination and enabling support staff all on site. - Scribing is available for interested providers; all providers have a 2:1 LPN/MA to provider ratio. - No administrative duties required. - Practice went through a workflow improvement program in January 2019 to improve provider satisfaction and work-life balance. - Watertown is a small city in a rural area with big-city conveniences. - Our community boasts a low cost of living, excellent schools, and a safe environment. - We experience four distinct seasons a year creating an excellent opportunity for recreational activities from white water rafting to skiing, and hiking to boating. - We are located 6 hours from New York City, and 3.5 hours from Montreal.

Physician / Urgent Care / Massachusetts / Locum tenens / Locum Tenens Urgent Care Opportunity available in Watertown, MA Pay $105/Hour Job

about 1 month ago
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StaffMD is seeking a Physician (MD/DO) for Locum Tenens coverage at an Urgent Care clinic located in Watertown, MA and Arlington, MA. Please see the details below and let me know if you are interested. Details: Dates: November 2017 (approximately 8-12 shifts) Will have ongoing needs. Family Medicine or someone whos worked in an urgent care setting (able to see all ages) BC Preferred but not required Part-time and full-time available candidates will be considered Pay Rate: $105/Hour Malpractice and Travel are covered. I look forward to hearing from you! Karl Sander StaffMD Locum Tenens and Permanent Placement p: 678-801-9301 m: 678-938-0118 w: www.StaffMD.com e: [email protected]

Full-Time: Lyft Driver - Earn $1650 Your First Month, Guaranteed - Join Lyft In Watertown, MA

about 2 months ago
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What is Lyft? Driving with Lyft is the perfect way to earn great money on any schedule (part-time, full-time, seasonal, hourly, or temporary) and Lyft Drivers can receive payment same-day through ...

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Become A Lyft Driver - Earn $1650 Your First Month, Guaranteed - Join Lyft In Watertown, MA. No C...

about 2 months ago
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What is Lyft? Driving with Lyft is the perfect way to earn great money on any schedule (part-time, full-time, seasonal, hourly, or temporary) and Lyft Drivers can receive payment same-day through ...

jobs byZipRecruiter

Internal Medicine, Internal Medicine Physician - Watertown, MA

about 1 year ago
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Elizabeth's Medical Center, Watertown, MA Steward Health Care System has created a model of exceptional quality and delivery of care for its patients AND a stimulating, progressive environment for ...

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Outpatient Psychiatrist Multi-Specialty Group (Part/Full time), Watertown, MA

about 2 years ago
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Part time or Fulltime Psychiatrist with a specialty in general adult behavioral health and substance abuse through an integrated patient care platform needed to provide between 10 40 hours per week ...

jobs byZipRecruiter

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