• Associate Director, Case Management Intake…

    CSL Behring (King Of Prussia, PA)
    …therapies that make a meaningful difference worldwide. We are looking for a ** Associate Director,** **Case Management Intake & Submissions** to join our R&D team. ... if required. . Close collaboration with WAVES team, IT, International Pharmacovigilance (IPV) & Capability Building and other interface functions to identify… more
    CSL Behring (12/05/25)
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  • Associate Director, PV Standards…

    CSL Behring (King Of Prussia, PA)
    …developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director, PV Standards and Governance? The job is in our King of ... establish and maintain global standards, policies, and governance frameworks for pharmacovigilance (PV) data and processes. You will ensure compliance, consistency,… more
    CSL Behring (01/08/26)
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  • Associate Medical Director, Clinical…

    Sumitomo Pharma (Harrisburg, PA)
    …a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The associate ... for INDs, NDAs, and other related documents. + Partner with Drug Safety & Pharmacovigilance to assess the safety profile of compounds. + Maintain a high level of… more
    Sumitomo Pharma (11/15/25)
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  • Associate Director, Marketing

    Merck (Montgomery County, PA)
    …in the Pipeline Advertisemen_ __ We are currently recruiting for several Associate Director positions within US Marketing, covering Physician (HCP), Consumer (HCC), ... **primary liaison** with commercial, medical affairs, market access, legal/compliance, pharmacovigilance , and external partners to ensure integrated program deployment.… more
    Merck (12/26/25)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
    The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... EMA, PMDA, ICH, etc. + General knowledge of global regulations for pharmacovigilance reporting for approved and investigational products. + Confirm list of upcoming… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Associate Principal Scientist, Clinical…

    Merck (North Wales, PA)
    …interacting with health agencies (eg FDA); understand key elements in pharmacovigilance , drug safety monitoring, signal detection and processing of adverse reports; ... (c) **Global Medical/Scientific Affairs:** Exposure to the management of a product asset prior to, during and after the launch phase (US and Global) including caveats on drug promotion. After a successful first year, the Physician Scientist will be equipped to… more
    Merck (01/10/26)
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  • Global Post Market Complaint Specialist II

    Dentsply Sirona (York, PA)
    …within the team. + Additional responsibilities as assigned. Education: + Associate 's degree required; Bachelor's degree preferred in fields including Life Sciences, ... experience in regulatory reporting, post-market surveillance, complaint handling, or pharmacovigilance in the medical device, pharmaceutical, or life sciences… more
    Dentsply Sirona (12/04/25)
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