• Associate Director , Clinical PV…

    Takeda Pharmaceuticals (Boston, MA)
    …in the business units and affiliates. + Ensure that the Global Quality Audit functions consider clinical research and pharmacovigilance regulated activities ... **OBJECTIVES:** + Provides oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities in the commercial business… more
    Takeda Pharmaceuticals (12/05/25)
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  • Associate Director , PV Sciences

    Taiho Oncology (Princeton, NJ)
    …Value Proposition: Embark on a transformative journey with Taiho Oncology as an Associate Director in PV Sciences. At the forefront of pharmacovigilance ... on your experience in our rapidly evolving organization. Position Summary: The Associate Director , PV Sciences role will lead medical surveillance activities… more
    Taiho Oncology (11/04/25)
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  • Associate Director , Market Research…

    Organon & Co. (Plymouth Meeting, PA)
    **Job Description** **Position Overview** The Associate Director is responsible for ensuring that Primary Market Research, Competitive Intelligence, and Data ... and procedures, and governing body rules and standards. The Associate Director will: + Be a champion...stakeholders in Commercial, Legal, Compliance, Privacy, Procurement, Business Technology, Quality & Audit, and Pharmacovigilance at all… more
    Organon & Co. (11/04/25)
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  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …is true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ... functional compliance teams for regulations impacting Clinical, Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and procedures and… more
    Takeda Pharmaceuticals (11/14/25)
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  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …is true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ... Quality team and share insights to trends to Clinical Pharmacovigilance and Medical Quality and R&D Quality leadership for proactive risk mitigation and… more
    Takeda Pharmaceuticals (10/14/25)
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  • Associate Director , ICSR Management…

    Ascendis Pharma (Princeton, NJ)
    …We offer a dynamic workplace for employees to grow and develop their skills. The Associate Director , ICSR Management Team reports to the Director , Head, ICSR ... the oversight of the PV Vendor processing ICSRs for Ascendis Products. + Performs Quality Checks of processed ICSRs and provides feedback to PV Vendor as applicable.… more
    Ascendis Pharma (10/09/25)
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  • Associate Director , Rare Blood…

    Sanofi Group (Cambridge, MA)
    **Job Title:** Associate Director , Rare Blood Disorders, Patient Services **Location:** Cambridge, MA **About the Job** Join the team transforming care for ... patients with some of the highest unmet needs. The Associate Director , Sutimlimab Patient Solutions will report...implementing services and education, how we can increase the quality and efficiency of these services. They will need… more
    Sanofi Group (11/20/25)
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  • Associate Director , Design Strategy…

    AbbVie (North Chicago, IL)
    …data and insights to the forefront of decision making via fit-for-purpose solutions. The Associate Director role in Data Science and Analytics is a leadership ... and advanced analytics techniques like Machine Learning and Artificial Intelligence. The Associate Director , Design Strategy and Engineering leads the UX/UI… more
    AbbVie (11/18/25)
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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 ... launch timeline. Key responsibilities for the _Physician Strategy Role:_ + Support Director HCP PMO to **drive foundational customer strategy** , leveraging L3… more
    Merck (09/26/25)
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  • Associate Director , Clinical Data…

    Xeris Pharmaceuticals, Inc. (Chicago, IL)
    …outsourcing, oversight and risk-based data management strategies, standards and processes. The Associate Director , Data Management will bring deep knowledge of ... checks) outsourced to CROs ensuring adherence to cost, timeline, and data quality requirements. * Participates in clinical vendor selection for external DM vendors… more
    Xeris Pharmaceuticals, Inc. (10/30/25)
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  • Associate Director , GCP Audit…

    Takeda Pharmaceuticals (Boston, MA)
    …best of my knowledge. **Job Description** **ABOUT THE ROLE** The Associate Director , GCP Audit & Compliance provides strategic quality oversight to clinical, ... leadership, supplier oversight, and strategic risk management to enhance end-to-end clinical quality . **HOW YOU CONTRIBUTE** + Lead strategic quality oversight… more
    Takeda Pharmaceuticals (11/21/25)
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  • Associate Director , Regulatory…

    Merck (Rahway, NJ)
    **Job Description** ** Associate Director , Regulatory Submissions Archive Operations** Location: Rahway, NJ (Hybrid role - onsite 3 days per week required) ... Management (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS) The Associate Director of Regulatory Submissions Archive Operations serves as the… more
    Merck (11/22/25)
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  • Associate Director , Program Manager

    Organon & Co. (Plymouth Meeting, PA)
    **Job Description** **The Position** We are looking for an experienced Associate Director , Program Manager to join our team. This successful candidate will ... and accurate program information in reports and systems to enable high quality portfolio communications. + Contribute to and facilitate an environment that fosters… more
    Organon & Co. (11/04/25)
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  • Associate Director , Regulatory…

    Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
    The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... intelligence management Standard Operating Procedures or work practices. + Review overall quality of ad hoc query research for requested regulatory topics and… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Sr. Director - PV Case Management ICSR

    Lilly (Indianapolis, IN)
    …life better for people around the world. **Job Responsibilities:** The Sr. Director PV Case Management ICSR provides technical leadership for the design, ... case management capabilities. The role oversees ICSR activities and case quality , including data analysis, trend reporting, KPIs, and business insights, while… more
    Lilly (12/03/25)
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  • Associate Medical Director /Medical…

    AbbVie (North Chicago, IL)
    …Participates in cross-functional teams to generate, deliver, and interpret high- quality clinical data supporting overall product scientific and business strategy. ... responses and discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality more
    AbbVie (11/18/25)
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  • Assoc Director , Patient Safety Medical…

    Gilead Sciences, Inc. (Foster City, CA)
    …individual to join the **Patient Safety Strategic Operations** team as an ** Associate Director , Patient Safety Medical Device Safety** responsible for supporting ... strategies and ensure operational excellence through successful business partner collaboration. The Associate Director , PS Medical Device Safety will be a… more
    Gilead Sciences, Inc. (10/16/25)
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  • Medical Director /Senior Medical…

    AbbVie (North Chicago, IL)
    pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research. Qualifications Medical Director ... Participates in cross-functional teams to generate, deliver, and interpret high- quality clinical data supporting overall product scientific and business strategy.… more
    AbbVie (10/09/25)
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  • Instructor for Master of Science (MS)…

    University of Maryland, Baltimore (Baltimore, MD)
    …of Pharmaceutical Sciences with teaching responsibility to the Graduate Program Director and Associate Dean for Graduate Programs. *_ACADEMIC RESPONSBILITIES ... science, including: Chemistry, Manufacturing, and Controls (CMC); Clinical Research; Pharmacovigilance ; Phase IV Research (eg, Pharmacoepidemiology); and Drug and… more
    University of Maryland, Baltimore (10/14/25)
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