• Global Pharmacovigilance (PV) Senior…

    Amgen (Washington, DC)
    safety / pharmacovigilance experience OR Bachelor's degree and 6 years of safety / pharmacovigilance experience OR Associate degree and 10 safety / ... with these qualifications. **Basic Qualifications:** Doctorate degree and 2 years of safety / pharmacovigilance experience OR Master's degree and 4 years of… more
    Amgen (11/09/24)
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  • Associate Director, Medical Safety

    Ascendis Pharma (Palo Alto, CA)
    …Key Responsibilities . Assists Head of Global Medical Safety Science for drug safety and pharmacovigilance activities for ensuring corporate compliance ... workplace for employees to grow and develop their skills. Associate Director, Medical Safety Science reports to...Safety Science, is responsible for all assigned Ascendis Drug Safety PV related activities for all… more
    Ascendis Pharma (11/28/24)
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  • Senior Patient Safety Physician - CRM…

    Boehringer Ingelheim (Ridgefield, CT)
    …or coach direct reports to 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 (10/12/24)
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  • Senior Patient Safety Physician - Oncology…

    Boehringer Ingelheim (Ridgefield, CT)
    …review of team output. + Provide updates of the assigned drug 's safety profile to senior management and recommend pharmacovigilance / risk management ... and expert team of physicians in the global Oncology Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of our… more
    Boehringer Ingelheim (11/16/24)
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  • Safety Surveillance Associate

    Pfizer (Collegeville, PA)
    …medicines for patients. **What You Will Achieve** Pfizer is excited to present a Safety Surveillance Associate opening within our Safety organization. In ... charge of reviewing, preparing, and completing reports of adverse drug experiences, to determine the safety profile...consequences. **Bonus Points If You Have** + Experience in pharmacovigilance , in clinical care, or in clinical or scientific… more
    Pfizer (11/27/24)
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  • Associate Director, Market Research…

    Takeda Pharmaceuticals (Lexington, MA)
    …my knowledge. **Job Description** **About the role:** Join Takeda as an Associate Director, Market Research and Competitive Intelligence, where you will be ... and accountability on all processes related to procurement, vendors, compliance, pharmacovigilance and budget management activities in execution of each CI and… more
    Takeda Pharmaceuticals (10/04/24)
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  • Associate Director, Quantitative Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …the cross-functional interfaces with key partners such as Pharmacometrics, Statistics, Drug Safety , Clinical Sciences, Outcomes, Digital Health, Pharmaceutical ... clinical pharmacology, statistics, programming, outcomes research and epidemiology, patient safety & pharmacovigilance , digital strategy, library sciences and… more
    Takeda Pharmaceuticals (10/11/24)
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  • Associate Director, Pharmacometrics Lead

    Takeda Pharmaceuticals (Boston, MA)
    …clinical pharmacology, statistics, programming, outcomes research and epidemiology, patient safety & pharmacovigilance , digital strategy, library sciences and ... order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director, Pharmacometrics Lead in Cambridge, MA, where you will lead and… more
    Takeda Pharmaceuticals (10/23/24)
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  • Associate Medical Director, Innovative…

    AbbVie (North Chicago, IL)
    …2+ years patient care experience strongly preferred + Minimum 2 years' experience in drug safety or a related discipline in the pharmaceutical industry + ... to pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk management plans + Contribute to… more
    AbbVie (09/20/24)
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  • Associate Director Process & Procedures…

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    …Departments: + Work closely with Integrated Operations (IOPs), BioAnalytical Systems (BAS), and Drug Safety and Pharmacovigilance (DSP) to ensure the EDMS ... The Associate Director, Systems Management is responsible for the strategic oversight and day-to-day management of systems that support the delivery of regulated… more
    Regeneron Pharmaceuticals (11/02/24)
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  • Associate Medical Director Immunology…

    AbbVie (North Chicago, IL)
    …integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is ... understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. May be… more
    AbbVie (11/14/24)
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  • Social Media Coordinator

    Bausch + Lomb (Rochester, NY)
    …Person for consumer-related issues escalated by team members + Manage communication within Drug Safety ( Pharmacovigilance ) email box + May collaborate with ... respond to the post or answer any questions: Regulatory- Pharmacovigilance , R&D, all other Bausch + Lomb sites worldwide,...use preferred and 1 year customer service experience + Associate or Bachelor's Degree preferred + Experience with the… more
    Bausch + Lomb (11/07/24)
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  • Senior Medical Director, Oncology/Hematology…

    AbbVie (North Chicago, IL)
    …integrity and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is ... limited supervision, for the proactive monitoring of clinical trial safety which is conducted in collaboration with the ABV...issues and queries. + May oversee the work of Associate Medical and/or Scientific Directors and of Clinical Scientists… more
    AbbVie (11/22/24)
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  • Sr. Director - ExploR&D Global Regulatory Affairs

    Lilly (Indianapolis, IN)
    …develop and test key scientific hypotheses, discharge risks regarding molecule safety and efficacy, and enable effective decision-making related to molecule ... including gap analysis and recommendations, advise on expedited pathways, orphan drug designation, and other regulatory advice meetings, and provide regulatory… more
    Lilly (11/23/24)
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  • Scientific Director, Clinical Scientist, Oncology…

    AbbVie (South San Francisco, CA)
    …training and clinical research experience to support all aspects of drug development, from facilitating the transition of molecules from pre-clinical discovery ... and communication of scientific data pertaining to the efficacy and safety of compounds in development. Attends conferences, reviews medical literature and… more
    AbbVie (09/25/24)
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  • Medical Director Clinical Development Eye Care

    AbbVie (Irvine, CA)
    …integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is ... and responses, and other program documents. + May oversee the work of Associate Medical and/or Scientific Directors, and of Clinical Scientists working on the same… more
    AbbVie (11/14/24)
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