• Director/Senior Associate Director, Medical…

    Boehringer Ingelheim (Ridgefield, CT)
    …disciplines as appropriate + Provide updates of the assigned drug 's safety profile to senior management and recommend pharmacovigilance / risk management ... team of physicians in the global Cardio-metabolism/Respiratory Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing… more
    Boehringer Ingelheim (07/13/24)
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  • Director, Medical Safety Assessment…

    Bristol Myers Squibb (Princeton, NJ)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Director, Medical Safety Assessment Physician (Immunology)** **Functional Area Description** ... Patient Safety (WWPS) group is responsible for ensuring the safety of our medicines. WWPS pharmacovigilance and pharmacoepidemiology deliverables include… more
    Bristol Myers Squibb (09/21/24)
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  • (Senior) Associate Director, Medical Safety

    Boehringer Ingelheim (Ridgefield, CT)
    **Description** The Medical Safety Physician will join our motivated and expert team of physicians in the global CNS, Retinopathy and Emerging Areas Therapeutic ... Area of Patient Safety and Pharmacovigilance at BI, whose priority...compounds. + Plan, manage / perform and monitor all pharmacovigilance activities for assigned drug responsibilities, including:… more
    Boehringer Ingelheim (09/24/24)
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  • Sr. Director, Regulatory Affairs/ Drug

    Merck (North Wales, PA)
    …pharmaceutical industry is required, with at least 5 years specifically involving safety experience (such as Pharmacovigilance or clinical work) involving direct ... **Job Description** Highly advanced understanding of safety and/or risk management to allow for overall accountability for the assigned cross-departmental process… more
    Merck (09/21/24)
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  • Early Development Clinical Research…

    Lilly (Indianapolis, IN)
    …and relevant therapeutic area experience , the Early Development Clinical Research Physician participates in the following: the development, conduct and reporting of ... and the reporting of adverse events as mandated by corporate patient safety ; the generation and review process for protocols, study reports, publications and… more
    Lilly (09/10/24)
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  • Clinical Pharmacologist/Clinical Research…

    Lilly (IN)
    …will have expertise in diabetes, obesity, cardiovascular renal or endocrinology drug development with demonstrated learning agility, a problem-solving mindset, and ... willingness to develop knowledge and skills in new areas. The Clinical Research Physician (CRP) will be the clinician to progress multiple early clinical assets into… more
    Lilly (09/17/24)
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  • Director, Pharmacovigilence Quality Oversight AI…

    Pfizer (New York, NY)
    …ensure the quality and reliability of AI systems that may affect pharmacovigilance . This involves contributing to and participating in various quality oversight ... to drive discussion and action related to mitigating risks to the pharmacovigilance system from the use of artificial intelligence. The incumbent leads PVQO… more
    Pfizer (09/26/24)
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  • Associate Director, Medical Safety

    Boehringer Ingelheim (Ridgefield, CT)
    …applicable and appropriate + Plan, manage / perform and monitor all pharmacovigilance activities for assigned drug responsibilities, including: + Continuous ... **Description** Associate Director has responsibility for the pharmacovigilance risk management activities for marketed and/or investigational compounds on a global… more
    Boehringer Ingelheim (09/24/24)
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  • Medical Safety Consultant- First Shift

    Randstad US (Philadelphia, PA)
    …(eg, nursing or pharmacy) or a relevant scientific/technical discipline and experience. skills: Pharmacovigilance , Drug Safety , DSUR (Development Safety ... Safety organization. In close collaboration with Medical Safety Physician and/or Medical Safety ...Requirements + At least 8 years of experience in drug safety , including at least 5 years… more
    Randstad US (09/25/24)
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  • Intern - Patient Safety , Oncology

    Gilead Sciences, Inc. (Foster City, CA)
    …and evaluation activities for assigned products in collaboration with the Global TA Safety Physician and Scientist as part of the continuous benefit-risk ... programs. **Position Overview** : You will learn about core Patient Safety Oncology pharmacovigilance activities, including signal detection, benefit-risk… more
    Gilead Sciences, Inc. (09/06/24)
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  • Late-Stage Clinical Development Leader

    Organon & Co. (Plymouth Meeting, PA)
    …feasible to execute, efficient and in line with Good Clinical and Good Pharmacovigilance Practice (GCP and GPvP). + Ensure excellent understanding of the external ... processes to secure an industry-benchmarked clinical development and clinical safety organization, operating in full compliance. + Ensure proactive intelligence… more
    Organon & Co. (09/10/24)
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