• Merck & Co. (Rahway, NJ)
    …for assigned protocols and sites in a country.Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country ... requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall… more
    HireLifeScience (05/02/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and ... Medical Writer on clinical/scientific and regulatory documents and the Study Manager on study deliverables.May provide tactical/scientific guidance to other clinical… more
    HireLifeScience (05/03/24)
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  • Pharmacovigilance Scientist, Senior

    Amgen (Washington, DC)
    …million patients worldwide. It's time for a career you can be proud of. ** Pharmacovigilance Scientist, Senior Manager ** **Live** **What you will do** Let's ... Be representative and point of contact for Health Authority Inspection and Internal Process Audits within the remit of role and responsibility + Processes and… more
    Amgen (05/02/24)
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  • 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 ... By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application… 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 , Drug Safety

    Mitsubishi Chemical Group (Jersey City, NJ)
    …closely with Drug Safety Global Safety Team (GST) Chair (Medical Director). The Manager , MSE will perform signal management process activities for assigned ... on real-world evidence, and creating hope for all facing illness. The Senior Managerwill support signal detection activities and medical analyses to support… more
    Mitsubishi Chemical Group (03/01/24)
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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 ... mange & mitigate risks, identify and mange deviation, define escalation process , and implement solutions in alignment with stakeholders and business partners.… more
    Sanofi Group (03/30/24)
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  • Senior Medical Director, Clinical Science,…

    Takeda Pharmaceuticals (Cambridge, MA)
    By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... to the best of my knowledge. **Job Description** **Job Description for Senior Medical Director, Clinical Science, Marketed Products Development** As the Senior more
    Takeda Pharmaceuticals (04/03/24)
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  • Senior Manager , Quality Management…

    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 ... advise on any issues to ensure compliance and for the Quality Risk Assessment process . + Ensuring and responsible for initiatives and process improvements, in… more
    Regeneron Pharmaceuticals (04/24/24)
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  • Senior Safety Associate III

    Randstad US (Cambridge, MA)
    senior safety associate iii. + cambridge , massachusetts + posted 7 days ago **job details** summary + $50.72 - $57.58 per hour + contract + bachelor degree + ... 57.58 per hour work hours: 9 to 5 education: Bachelors responsibilities: The Senior Safety Associate III will be responsible for supporting Global Case Management… more
    Randstad US (04/28/24)
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  • Senior Clinical Research Associate - NH,…

    Merck (Columbus, OH)
    …for assigned protocols and sites in a country. Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country ... requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall… more
    Merck (05/01/24)
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  • Senior Clinical Scientist- Cardiovascular…

    Merck (North Wales, PA)
    **Job Description** Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical ... the Medical Writer on clinical/scientific and regulatory documents and the Study Manager on study deliverables. + May provide tactical/scientific guidance to other… more
    Merck (05/03/24)
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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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  • Audit Manager , Research Development…

    Pfizer (Tampa, FL)
    **Role Summary** The Audit Manager , Research, Development and Supply will be part of Pfizer Corporate Audit's internal team that provides "third line of defense" ... Chain to plan and execute best in class audit assurance. The Audit Manager is responsible for identifying risks in specific business areas and conducting independent… more
    Pfizer (05/03/24)
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  • Region Associate Director / Region Director,…

    Bristol Myers Squibb (Minneapolis, MN)
    …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 ... and across therapeutic areas (TA) + Identifies talent, conducts robust interview process for selecting highly qualified FM and other Medical personnel, and fills… more
    Bristol Myers Squibb (04/10/24)
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  • Associate Director, Clinical Quality Operations,…

    Merck (Columbus, OH)
    **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... and Head of Clinical Quality Operations (HCQO), the Clinical Quality Operations Manager (CQOM)} is responsible for the execution of operational quality activities… more
    Merck (04/24/24)
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  • Director, Global Regulatory Strategy Lead…

    Boehringer Ingelheim (Ridgefield, CT)
    manager is not based in the country you are applying for and the interview process is performed in the hiring manager country, we kindly urge you to opt for ... the country you are applying for and the interview process is performed in the hiring manager ...team members, encourage cross-functional coordination and coordinate with the ( senior ) regulatory project manager to achieve regulatory… more
    Boehringer Ingelheim (04/18/24)
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