• Merck & Co. (Rahway, NJ)
    …Training Programs, FDA Regulations, IT Coordination, IT Operation, Pharmacovigilance , Policy Implementation, Regulatory Compliance, Regulatory Labeling, Regulatory ... Operations, Regulatory Submissions, Strategic Thinking {+ 1 more}Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can engage… more
    HireLifeScience (12/11/25)
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  • Merck & Co. (Montgomery County, PA)
    …described in the Pipeline Advertisemen We are currently recruiting for several Associate Director positions within US Marketing, covering Physician (HCP), ... the launch timeline.Key responsibilities for the Physician Strategy Role: Support Director HCP PMO to drive foundational customer strategy, leveraging L3 marketing… more
    HireLifeScience (09/26/25)
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  • Lupin Pharmaceuticals (Coral Springs, FL)
    …safety signals, adverse events, and efficacy data in collaboration with pharmacovigilance teams. Target Product Profile (TPP) Contributions: Develop and refine TPPs ... by outlining desired product characteristics such as indications, target population, dosing regimen, safety profile, and clinical efficacy.Align TPPs with regulatory requirements and commercial goals to guide product development strategies. Due Diligence… more
    HireLifeScience (09/15/25)
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  • 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...Compliance, Privacy, Procurement, Business Technology, Quality & Audit, and Pharmacovigilance at all levels of our business. + Maintain… more
    DirectEmployers Association (11/05/25)
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  • 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 ... onsite and remote work schedule_ _. #LI-hybrid_ **The Role:** Reporting to the Sr. Director , Global Case Management, you will: + Oversee intake and triage of all… more
    DirectEmployers Association (12/05/25)
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  • Parexel (Tallahassee, FL)
    …success, we are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and ... Inflammation Therapeutic Franchise. As an Associate / Medical Director , you will work...needed with the support of the designated Senior Medical Director / Global Head of TA (as appropriate) Pharmacovigilance more
    DirectEmployers Association (10/10/25)
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  • 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 ... in R&D functions (eg, Clinical Research, Early Development, Medical Affairs, Pharmacovigilance , Regulatory Affairs, etc.) + At least three years of experience… more
    DirectEmployers Association (11/04/25)
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  • Senior Patient Safety Physician, Medical Safety…

    Boehringer Ingelheim (Ridgefield, CT)
    **Description** Director OR Senior Associate Director has responsibility for the pharmacovigilance risk management activities of marketed and/or ... subspecialty would be an asset. + People leadership potential required. Senior Associate Director : + Total applicable experience (incl. clinical practice, plus… more
    Boehringer Ingelheim (11/05/25)
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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 , Clinical PV…

    Takeda Pharmaceuticals (Boston, MA)
    …**OBJECTIVES:** + Provides oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities in the commercial business ... affiliate and enables them to deliver their clinical research and pharmacovigilance -related regulated activities with high compliance and agility. + Establish and… more
    Takeda Pharmaceuticals (12/12/25)
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