• Senior Clinical Data Scientist

    Boehringer Ingelheim (Ridgefield, CT)
    **Description** Senior Clinical Data Scientist at Boehringer Ingelheim Pharmaceuticals, Inc. in Ridgefield, CT (Telecommuting permitted: work may be performed in any ... level, including colleagues from Global Clinical Operations (GCO), Global Pharmacovigilance (GPV), TAs, Translational Medicine and Clinical Pharmacology (TMCP), and… more
    Boehringer Ingelheim (06/26/25)
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  • Senior Principal Scientist , Clinical…

    Merck (Rahway, NJ)
    **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... Intellectual Curiosity, Interdisciplinary Problem Solving, Mentorship, Neuroanatomy, Pharmaceutical Development, Pharmacovigilance , Psychiatry, Regulatory Affairs Compliance, Regulatory Compliance, Regulatory Requirements,… more
    Merck (07/31/25)
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  • Senior Principal Scientist , Project Team…

    Boehringer Ingelheim (Ridgefield, CT)
    …& Clinical Pharmacology, CMC, Regulatory Affairs, Patient Safety and Pharmacovigilance to implement discovery and development toxicology strategies that enable ... the progression of optimized drug candidates. + When appropriate, take lead to develop plan and lead sub-team for investigative studies to support investigations on mechanisms of toxicity. + Serve as NDS Therapeutic Area lead, and/or provide guidance and… more
    Boehringer Ingelheim (07/10/25)
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  • Senior Director - GPS Benefit-Risk Management…

    Lilly (Indianapolis, IN)
    …and in support of the European Union Qualified Person for Pharmacovigilance (EU QPPV). **Benefit-Risk Management** **Leadership** **1) End-to-End Business Process ... internal expert to provide specialized knowledge within the area of Pharmacovigilance risk management and risk minimization activities. + Collaborate with… more
    Lilly (06/25/25)
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  • SR Clinical Research Associate

    Boehringer Ingelheim (Athens, GA)
    …(AE) reporting and request primary and follow-up information. + Provides information to pharmacovigilance and RA according to the study protocol and SOPs. + Ensures ... Regulatory Affairs to align on document organization. + Collaborates with the Scientist and study team in protocol development, CRF design, writing amendments,… more
    Boehringer Ingelheim (07/11/25)
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  • Executive Medical Director, Oncology Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …Development Team but more likely will oversee the study physician and/or clinical scientist leads responsible for leading the team. Emphasis will be on insuring that ... compounds. + Reviews and assesses overall safety information in conjunction with Pharmacovigilance and Medical Monitor of record for assigned compounds. + Oversees… more
    Takeda Pharmaceuticals (07/28/25)
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  • Vice President, DCTL, Sonrotoclax

    BeOne Medicines (San Mateo, CA)
    …clinical development, program leadership, biometrics, clinical operations, safety/ pharmacovigilance , regulatory, molecular diagnostics, and translational research. ... at least one study through from start to finish in a clinical scientist role + Clinical oncology experience; candidates with exceptional experience in other… more
    BeOne Medicines (07/24/25)
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  • Executive Medical Director, Clinical Development

    Taiho Oncology (Princeton, NJ)
    …the development program. + Perform data review supported by Clinical Research Scientist (s) (CRS), participate in protocol deviation meeting that will occur monthly ... cross-functional areas (eg, clinical operations, biostatistics, data management, biomarker, pharmacovigilance , quality, etc.) + Knowledge in authoring key clinical… more
    Taiho Oncology (06/25/25)
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