• Associate Director

    Lilly (Indianapolis, IN)
    …to make life better for people around the world. The purpose of the Associate Director PV Systems Strategy and Implementation is to develop, implement, and ... automation, technology and analytics needs. + Maintain deep technical understanding of safety process knowledge in order apply technology and automation to PV… more
    Lilly (01/13/26)
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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 ... Safety Database. + Reviews and provides input to Business Partner or Pharmacovigilance Agreements and Safety Data Exchange Agreements (SDEA) to ensure… more
    Ascendis Pharma (01/07/26)
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  • Associate Medical Director /Medical…

    ThermoFisher Scientific (Greenville, NC)
    …(comparable to 1-2 years) in the industry; Or + Direct experience in safety / Pharmacovigilance (comparable to 2 years) **For Medical Director Level:** + MD or ... comprehensive background check, which includes a drug screening. Our detailed, goal-oriented Pharmacovigilance colleagues manage the safety profile of new drugs… more
    ThermoFisher Scientific (12/09/25)
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  • Associate Medical Director

    ThermoFisher Scientific (Greenville, NC)
    …(comparable to 1-2 years) in the industry; Or + Direct experience in safety / Pharmacovigilance medical monitoring (comparable to 2 years). + For Medical ... Director Level candidates should have Clinical experience in treating...years) in the industry; Or + Direct experience in safety / Pharmacovigilance (comparable to 2+ years) + Preferences… more
    ThermoFisher Scientific (01/07/26)
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  • Associate Director , Case Management…

    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 ... accurate and timely entry of reports into the global safety database by the vendor. Under Case Submissions, you...schedule_ _. #LI-hybrid_ **The Role:** Reporting to the Sr. Director , Global Case Management, you will: + Oversee intake… more
    CSL Behring (12/05/25)
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  • Associate Director , Clinical…

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

    Astellas Pharma (Northbrook, IL)
    …teams. 1. ** Pharmacovigilance (6 months)** + Develop hands-on experience in safety monitoring and risk management throughout the drug lifecycle. + Develop an ... diverse rotations-Clinical Development (12 months), Medical Affairs (6 months), and Pharmacovigilance (6 months), Participants will gain hands-on exposure to key… more
    Astellas Pharma (12/04/25)
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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 ... Health, or a related field​ + 10+ years of experience in pharmacovigilance , safety data management, or regulatory affairs​ + Knowledge of global PV regulations,… more
    CSL Behring (01/08/26)
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  • Associate Medical Director

    Sumitomo Pharma (Annapolis, MD)
    …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director , Clinical Development - Oncology** . The ... associate medical director is responsible for the leadership, development, and management...NDAs, and other related documents. + Partner with Drug Safety & Pharmacovigilance to assess the … more
    Sumitomo Pharma (11/15/25)
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  • Associate Director , Structured…

    Bristol Myers Squibb (Madison, NJ)
    …your application should be directed to Chat with Ripley. R1596641 : Associate Director , Structured Benefit-Risk Assessment Lead **Company:** Bristol-Myers Squibb ... (SBRA) Lead will report into the Structured Benefit-Risk Assessment Head within Safety Evidence and Sciences and will be accountable to lead structured benefit-risk… more
    Bristol Myers Squibb (01/11/26)
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  • Associate Director , Biostatistics…

    BeOne Medicines (San Mateo, CA)
    …CSM statistician interfacing with clinical study statisticians, medical monitors, safety / pharmacovigilance , global clinical operations (GCO), quality/GCP, data ... design, interpretation, and governance for monitoring activities that protect subject safety , ensure data integrity, and support trial reliability across BeOne's… more
    BeOne Medicines (01/14/26)
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  • Senior Patient Safety Physician, Medical…

    Boehringer Ingelheim (Ridgefield, CT)
    **Description** Director OR Senior Associate Director has responsibility for the pharmacovigilance risk management activities of marketed and/or ... team output. + Provide updates of the assigned drug's safety profile to senior management and recommend pharmacovigilance...be an asset. + People leadership potential required. Senior Associate Director : + Total applicable experience (incl.… more
    Boehringer Ingelheim (11/05/25)
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  • Associate Director , Statistics

    Takeda Pharmaceuticals (Boston, MA)
    …Sciences, Statistics & Quantitative Sciences, Programming, Global Evidence Outcomes, Patient Safety & Pharmacovigilance , and Strategic Operations The department ... integrates data science, analytics, and quantitative methods to enhance efficiency and precision throughout the drug discovery and development lifecycle. It leverages cutting-edge technology, machine learning, AI, and statistical methods to analyze complex… more
    Takeda Pharmaceuticals (12/11/25)
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  • (Senior) Patient Safety Physician, Medical…

    Boehringer Ingelheim (Ridgefield, CT)
    …conclusions. + Understanding of the pharmaceutical industry and regulatory environment. **Requirements** Associate Director Requirements: + US MD or DO degree or ... **Description** (Senior) Patient Safety Physician has responsibility for the pharmacovigilance...more than 2 years of applicable experience, required. Sr. Associate Director Requirements: + US MD or… more
    Boehringer Ingelheim (01/14/26)
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