• Director, Clinical Science- GI2 TAU

    Takeda Pharmaceuticals (Cambridge, MA)
    …Recommends high impact global decisions. + Responsible for monitoring and interpreting data from ongoing internal and external studies, assessing the medical and ... scientific rigor and integrity of clinical trials is maintained and that the resulting data are of high quality to allow data -driven decision-making. In this… more
    Takeda Pharmaceuticals (05/14/25)
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  • Global Medical Lead Entyvio(R)

    Takeda Pharmaceuticals (Cambridge, MA)
    …The incumbent will display high scientific and ethical standards. **KEY ACCOUNTABILITIES:** ** Data generation** + Contributes to the clinical strategy and leads key ... flagship programs, including the data generation plan which includes both clinical and non-clinical projects + Contributes to Phase 3b/4 research and RW data more
    Takeda Pharmaceuticals (05/10/25)
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  • Senior Manager, Programming

    Takeda Pharmaceuticals (Boston, MA)
    …study, organize and prioritize programming activities including production and quality control of datasets and outputs while following internal standard operating ... Study Execution Team (SET) meetings; oversee external clinical research organization ( CRO ) to ensure they meet programming milestones/timelines and high quality of… more
    Takeda Pharmaceuticals (04/05/25)
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  • Senior Clinical Scientist

    Sanofi Group (Cambridge, MA)
    …(eg pressure test and cluster feasibility, medical review and validation of clinical data , study risk assessment) + Contribute to the Abbreviated Protocol, the final ... to clinical studies such as medical training, feasibility, medical review of data , medical information for the study team, medical advisors/Clinical Project Leaders… more
    Sanofi Group (05/15/25)
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  • Manager Of Programming, Statistics

    Actalent (Waltham, MA)
    …programming activities across various studies and programs, ensuring high-quality clinical data and analysis are delivered timely and within budget. Responsibilities ... contracted vendors or vendor groups within CROs to ensure data and analyses are complete, accurate, and delivered on...Minimum of 5 years of experience in pharmaceutical or CRO environments, including Phase I, II, and III studies.… more
    Actalent (05/19/25)
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  • ASO Scientist

    Eurofins (Cambridge, MA)
    …leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders ... using Client instrumentation and supplies. Technical feedback and final review of data are the responsibilities of Client personnel, but all performance feedback and… more
    Eurofins (05/09/25)
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  • Principal Scientist I - Discovery Bioanalysis

    Charles River Laboratories (Worcester, MA)
    …method development and execution of quantitative assays, critical review of data , mentoring junior staff, and maintaining analytical equipment. Individuals in this ... The scientist is expected to work independently to deliver high-quality non-GLP data in a fast-paced environment. The successful candidate in this position will… more
    Charles River Laboratories (04/09/25)
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  • Scientist

    Sanofi Group (Cambridge, MA)
    …as responsible scientist for regulated studies; provide scientific oversight and data interpretation and ensure data meets compliance requirements according ... standard operating procedures, study plans and reports, and abstracts; present scientific data to fellow colleagues + Take a leadership role in ensuring regulatory… more
    Sanofi Group (05/22/25)
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  • Clinical Pathology Technician I

    Charles River Laboratories (Shrewsbury, MA)
    …received into the laboratory. Maintain and perform record keeping. Review raw data for quality control . **ESSENTIAL DUTIES AND RESPONSIBILITIES:** * Perform ... and process BA/TK samples. * Manual entry of raw data into computerized systems and review of data...River** Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of laboratory… more
    Charles River Laboratories (05/15/25)
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  • Director, Clinical Biomarker, Late Stage Neurology…

    Bristol Myers Squibb (Cambridge, MA)
    …and ensuring appropriate collection and timely analysis and reporting of final biomarker data . The individual will also be responsible for answering key TM questions ... creation of clinical protocols, SAPs, SOWs, lab manual, and interfacing with CRO for execution of services, in conjunction with Biospecimen Operations and… more
    Bristol Myers Squibb (05/07/25)
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