• Associate Medical Director/Medical Director…

    ThermoFisher Scientific (Greenville, NC)
    …find cures for cancer. **Location/Division Specific Information** Our detailed, goal-oriented Pharmacovigilance colleagues manage the safety profile of new drugs in ... to 1-2 years) in the industry; Or + Direct experience in safety/ Pharmacovigilance (comparable to 2 years) + Experience preference towards individuals with clinical… more
    ThermoFisher Scientific (07/15/25)
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  • Senior Medical Director - Rheumatology

    ThermoFisher Scientific (Greenville, NC)
    …required). **Discover Impactful Work:** Advanced leadership responsibilities within the Pharmacovigilance (PV) physician team which may include direct line ... organization on significant matters. + Utilizes subject matter clinical and pharmacovigilance expertise, combined with knowledge of the product(s) or therapeutic… more
    ThermoFisher Scientific (07/15/25)
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  • Compliance Operations Lead, Associate Director…

    Takeda Pharmaceuticals (Boston, MA)
    …CPMQ activities eg audit, inspection, QE, CAPA. + Organise Clinical and Pharmacovigilance Quality council meetings and proactively manage the agenda and ensure key ... include successful development and implementation of a clinical or pharmacovigilance audit program, hosting/leading regulatory inspections, investigations and remediation… more
    Takeda Pharmaceuticals (07/12/25)
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  • Director, GCP Audits

    Gilead Sciences, Inc. (Parsippany, NJ)
    …in cross-functional projects and teams with responsibilities related to pharmacovigilance and quality system activities. + Significant experience leading quality, ... industry, including significant relevant experience working in quality, compliance, pharmacovigilance , or a related field. + Extensive experience leading GCP… more
    Gilead Sciences, Inc. (06/27/25)
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  • Consulting Manager - Life Sciences (Remote)

    Cognizant (Austin, TX)
    …execution across areas such as Clinical Operations, Regulatory Affairs, Pharmacovigilance , and Quality. **Key Responsibilities** **Domain Expertise** : Serve as ... exposure to one or more functions: Clinical Development, Regulatory Affairs, Pharmacovigilance , Quality, or Commercial Operations. Proven track record in process… more
    Cognizant (06/21/25)
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  • Future Opportunities - Join Our Talent Pipeline…

    AbbVie (North Chicago, IL)
    …study protocols and informed consents. When appropriate write the key pharmacovigilance documents, including but not limited to, medical safety assessments, ... residency with patient management experience 2. 5 - 8 years of Pharmacovigilance / Clinical Development experience in the pharmaceutical industry 3. Effectively… more
    AbbVie (06/19/25)
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  • Vice President, Head of Regulatory Legal

    Lilly (IN)
    …Affairs, Manufacturing & Quality (including Environmental), Global Patient Safety or pharmacovigilance , Clinical Development and other functions and teams. The ideal ... law including manufacturing, supply chain, clinical design, clinical trials, and pharmacovigilance . Qualifications: + Juris Doctor (JD) degree from an accredited law… more
    Lilly (06/11/25)
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  • Global Safety Officer, Rare

    Sanofi Group (Cambridge, MA)
    …safety input into development plans + Support due diligence activities and pharmacovigilance agreements Impact: + Ongoing assessment of the safety status of the ... minimum of 3 years in total experience in international or large market pharmacovigilance , or at least 4 years of clinical development experience + Exceptionally,… more
    Sanofi Group (06/05/25)
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  • Senior Director, Global Process Owner - Quality…

    Lilly (Durham, NC)
    …working in at least two of Clinical Operations / Development, Pharmacovigilance , Product Research & Development or Commercial Manufacturing preferred. **A** ... **dditional Information:** + Available to travel (domestic and international) when required. + Fluent in English, additional languages are also recommended. + Role may be based at selected Lilly Locations in Europe or the US. Lilly is dedicated to helping… more
    Lilly (08/02/25)
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  • Manager, Device Safety Associate

    J&J Family of Companies (Raritan, NJ)
    …4 years of combined experience and post-baccalaureate education in pharmacovigilance , device safety, or biomedical/systems engineering (with demonstrated medical ... device experience) is required + Ability to effectively drive cross-disciplinary, highly matrixed teams to meet safety and compliance objectives for device assets is required + Ability to rapidly assimilate and apply new information for device assets and… more
    J&J Family of Companies (08/02/25)
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