• Senior Manager

    Takeda Pharmaceuticals (Lexington, MA)
    …my knowledge. **Job Description** Takeda Development Center Americas, Inc. is seeking a Senior Manager , Pharmacovigilance (PV) Business Partner Relations in ... of related experience. Required skills: Review and provide input on Pharmacovigilance Agreements (PVAs) and associated business agreements; analyze and provide… more
    Takeda Pharmaceuticals (02/28/24)
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  • Senior Manager , Safety Scientist

    BeiGene (Emeryville, CA)
    …departmental activities **Supervisory Responsibilities:** + The position has no direct reports. The Senior Manager , Safety Scientist is part of a team that ... + Assist with integrated Benefit/Risk assessments **Promote and Advance the Field of Pharmacovigilance ** + Any other tasks assigned by manager to assist in… more
    BeiGene (04/03/24)
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  • Senior Manager , Quality

    Regeneron Pharmaceuticals (Armonk, NY)
    The Senior Manager , Global Development Quality Management (GCP) acting as a Quality Management Lead (QML) is a key position that will provide mentorship ... and leadership for all aspects of quality and compliance. The incumbent will engage with key...transferable skills related to Good Clinical Practice(GCP), and/or Good Pharmacovigilance Practice (GVP). Does this sound like you? Apply… more
    Regeneron Pharmaceuticals (04/24/24)
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  • Senior Manager , Drug Safety

    Mitsubishi Chemical Group (Jersey City, NJ)
    …on real-world evidence, and creating hope for all facing illness. The Senior Managerwill support signal detection activities and medical analyses to support ... with Drug Safety Global Safety Team (GST) Chair (Medical Director). The Manager , MSE will perform signal management process activities for assigned products,… more
    Mitsubishi Chemical Group (03/01/24)
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  • Senior Medical Director, Clinical Science,…

    Takeda Pharmaceuticals (Cambridge, MA)
    …to the best of my knowledge. **Job Description** **Job Description for Senior Medical Director, Clinical Science, Marketed Products Development** As the Senior ... and partners with marketed products R&D function leads (regulatory affairs, pharmacovigilance , global development operations and project management) to set R&D… more
    Takeda Pharmaceuticals (04/03/24)
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  • Global Senior Manager - Governance…

    Sanofi Group (Cambridge, MA)
    …treatment to patients with specific illnesses where treatment access is limited. **Global Senior Manager - Governance & Risk Management** sits within Specialty ... EAP programs management. + Significant experience in Medical Governance, Medical Quality , Pharmacovigilance , Regulatory Affairs, Medical Operations (at global… more
    Sanofi Group (03/30/24)
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  • Director/ Senior Associate Director,…

    Boehringer Ingelheim (Ridgefield, CT)
    …etc.). Senior CPL will liaise with the Digital Content Manager regarding new tools/technologies/best practices. + Provides input into Medical Affairs strategy ... **Description** The role of Senior Clinical Program Leader (CPL) - Retinal health,...The incumbent will drive patient value, patient voice and quality of life & outcomes in line with Medicine… more
    Boehringer Ingelheim (02/27/24)
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  • Regulatory And PV Compliance

    Randstad US (Trenton, NJ)
    …executing global Regulatory and PV compliance activities. - Identify and escalate critical quality issues to senior GRADS Compliance management. - Support (as ... regulations, procedures, and contractual requirements. Through the implementation of quality and compliance tracking tools/reports, oversight strategy, and relationship… more
    Randstad US (04/17/24)
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  • Associate Director, Clinical Quality

    Merck (Columbus, OH)
    …Lead {CQOL and Head of Clinical Quality Operations (HCQO), the Clinical Quality Operations Manager (CQOM)} is responsible for the execution of operational ... **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety...indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying… more
    Merck (04/24/24)
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  • Sr. Clinical Study Manager

    Kedrion Biopharma, Inc. (Fort Lee, NJ)
    …agreed-upon timelines and budget, while ensuring patient safety and data quality . To support and contribute to ongoing process improvement workstreams. **MANAGEMENT ... are completed for assigned clinical trials to agreed timelines, budgets and data quality standards. Activities include but are not limited to the following: +… more
    Kedrion Biopharma, Inc. (01/30/24)
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  • Manager , Safety Statistical Programming

    AbbVie (Boston, MA)
    …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Manager of Safety Statistical Programming is a strategic role in the emerging ... of integrated clinical safety data for multiple compounds and indications. The Manager of Safety Statistical Programming must effectively interface with team members… more
    AbbVie (04/24/24)
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  • Region Associate Director / Region Director,…

    Bristol Myers Squibb (Chicago, IL)
    …and payers. The RD position is also responsible for working closely with senior management to create and execute medical initiatives at a national level. This ... leadership commitment and role modelling of the highest standards of quality , compliance, uncompromising ethics and integrity. **Leading and Managing Field Medical… more
    Bristol Myers Squibb (04/10/24)
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  • Director, Global Regulatory Strategy Lead…

    Boehringer Ingelheim (Ridgefield, CT)
    …among team members, encourage cross-functional coordination and coordinate with the ( senior ) regulatory project manager to achieve regulatory milestones & ... apply to, or be accessible to any company recruiter worldwide. Given that the hiring manager is not based in the country you are applying for and the interview… more
    Boehringer Ingelheim (04/18/24)
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  • Executive Medical Director Oncology Clinical…

    AbbVie (North Chicago, IL)
    …Strategy Teams (CSTs) and clinical study teams, to ensure high- quality , cross-functionally-aligned program (ie, Clinical Development Plan) and study deliverables ... strategies at a disease area and platform level. + Acts as a senior -level liaison for opinion leader interactions related to the disease area(s); partners with… more
    AbbVie (04/16/24)
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  • Vice President, Clinical Development

    Editas Medicine (Cambridge, MA)
    …messaging and communication strategies. The incumbent is expected to be a strong people manager and be willing to 'roll up the sleeves' as needed to accomplish ... pre-IND activities to BLAs, establishing plans for long-term follow up and pharmacovigilance , and is responsible for protocol development and clinical sections of… more
    Editas Medicine (03/07/24)
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