• Associate Director, Clinical and Safety…

    Takeda Pharmaceuticals (Boston, MA)
    …Management and Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical development, medical affairs ... **About the role:** The Associate Director, Clinical and Safety Quality Compliance is responsible for ensuring the quality...and GCP /GVP regulations including FDA, EU, MHRA, PMDA and ICH.… more
    Takeda Pharmaceuticals (07/25/25)
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  • Associate Director, Clinical Program…

    Takeda Pharmaceuticals (Boston, MA)
    …Management and Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical development, medical affairs ... **Job Description** **About the role:** Associate Director, Clinical Program Quality Investigations is responsible for ensuring the compliance of...and GCP /GVP regulations including FDA, EU, MHRA, PMDA and ICH.… more
    Takeda Pharmaceuticals (07/16/25)
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  • Compliance Operations Lead, Associate Director…

    Takeda Pharmaceuticals (Boston, MA)
    …Management and Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical development, medical affairs ... of my knowledge. **Job Description** **OBJECTIVES:** + Ensures Global and R&D Quality processes are embedded and effectively implemented across CPMQ + Partner with… more
    Takeda Pharmaceuticals (08/08/25)
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  • Pricing Analyst Sr - Strong SQL/ GCP…

    Prime Therapeutics (Boston, MA)
    …every decision we make. **Job Posting Title** Pricing Analyst Sr - Strong SQL/ GCP - Remote **Job Description** The Senior Pricing Analyst participates in the ... **Preferred Qualifications** + Prior experience with Google Cloud Platform ( GCP ) and BigQuery (or another SQL tool such as...new ideas and work collaboratively to provide the highest quality of care and service to our members. If… more
    Prime Therapeutics (08/01/25)
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  • Cloud Engineer ( GCP )

    Prime Therapeutics (Boston, MA)
    …our passion and drives every decision we make. **Job Posting Title** Cloud Engineer ( GCP ) **Job Description** + As a Data Engineer (Systems Developer) you will be ... Analyze and recommend changes to improve efficiency, performance, lower costs, and enhance quality of data assets + Work with System Analysts, Technical Leads, and… more
    Prime Therapeutics (08/12/25)
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  • Senior Manager, Study Management

    Takeda Pharmaceuticals (Boston, MA)
    …the execution of studies in a matrix management structure to ensure compliance with quality standards (including ICH GCP , local regulations and Takeda SOPs). + ... management team members in order to deliver operational consistency and high quality support across clinical trial programs. + Provide guidance and mentorship to… more
    Takeda Pharmaceuticals (08/20/25)
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  • Head of Biospecimen Management

    Sanofi Group (Cambridge, MA)
    …local teams to manage clinical samples according to health authority guidelines and quality requirements defined in GLP/ GCP . + Liaises with the clinical study ... are collected, shipped, processed, analyzed, and stored with the highest degree of quality and in compliance with applicable regulations. + Tracking and managing all… more
    Sanofi Group (06/13/25)
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  • Senior Research Manager, US Medical

    Takeda Pharmaceuticals (Lexington, MA)
    …and external resource activities to ensure Company Sponsored studies are conducted in GCP compliant and quality manner following all company processes and ... applicable laws. + Support Study Execution Team to lead Company Sponsored Studies forward to achieve objectives within target timelines and budget. + Support study contracts and finances including budget forecasting, contract execution and management, change… more
    Takeda Pharmaceuticals (08/22/25)
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  • Executive Director of R&D Global Quality…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …Summary** We are seeking an experienced and dynamic Executive Director of R&D Global Quality to join our team. This pivotal role will be responsible for leading a ... global team focused on R&D Quality . This global role includes direct reports in the...compliance with applicable regulations and guidelines that ensure sustained GCP /QSR compliance. + **Vendor Management:** Leads and develops systems… more
    Otsuka America Pharmaceutical Inc. (08/14/25)
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  • Human Research Quality Manager, School…

    Boston University (Boston, MA)
    **HUMAN RESEARCH QUALITY MANAGER, School of Medicine, Clinical Research** **Job Description** **HUMAN RESEARCH QUALITY MANAGER, School of Medicine, Clinical ... Type** Full-Time/Regular The Human Research Protection Program (HRPP) Human Research Quality Manager will perform quality assurance monitoring and auditing… more
    Boston University (07/09/25)
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