• Director , Global Health Economics, Value,…

    Teva Pharmaceuticals (Parsippany, NJ)
    Director , Global Health Economics, Value, and Outcomes - In-line Brands (Parsippany, NJ) Date: Aug 6, 2025 Location: Parsippany, United States, New Jersey, 07054 ... and new people to make a difference with. **The opportunity** As the Director , In-line Brands - Global Health Economics, Value, and Outcomes, you will serve… more
    Teva Pharmaceuticals (08/08/25)
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  • Associate Medical Director

    Sumitomo Pharma (Trenton, NJ)
    …highly motivated, and experienced individual for the position of **Associate Medical Director .** The Associate Medical Director will provide hands-on PVRM ... products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs), including… more
    Sumitomo Pharma (08/15/25)
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  • Associate Director , Statistics - (Hybrid)

    AbbVie (Florham Park, NJ)
    …IL; San Francisco, CA; Irvine, CA; Florham Park, NJ The Associate Director , Statistics provides statistical leadership for clinical development and life-cycle ... management strategies for assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs. The Associate … more
    AbbVie (08/30/25)
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  • Director Regulatory Affairs

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …self. Become a **maker of possible** with us. The Regulatory Affairs (RA) Director is responsible for the management and setting the direction for the Medication ... platform within the Medication Delivery Solution Business Unit. The RA Director is responsible for developing and implementing regulatory strategies and submissions… more
    BD (Becton, Dickinson and Company) (08/08/25)
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  • Associate Director , Quantitative…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …may be considered within the US. As an **Associate Director , Quantitative Pharmacology, Pharmacometrics,** you will support all **pharmacometrics** activities ... dose optimization, exposure-response and pediatric development. You will Author clinical pharmacology and **pharmacometrics** submission documents and represent the… more
    Otsuka America Pharmaceutical Inc. (08/16/25)
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  • Executive Director of R&D Global Quality…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    **Job Summary** We are seeking an experienced and dynamic Executive Director of R&D Global Quality to join our team. This pivotal role will be responsible for ... Quality will ensure OAPI, OPDC and all affiliates are inspection ready, oversee clinical trial and submission support, lead the R&D audit program, engage with… more
    Otsuka America Pharmaceutical Inc. (08/14/25)
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  • Assoc. Director , EEG

    PsychoGenics (Paramus, NJ)
    Assoc. Director , EEG **PsychoGenics** is a preclinical CRO with expertise in central nervous system (CNS) and orphan disorders. Our mission is to provide the best ... and orphan disorders and reduce the attrition rate in clinical development. We are known for our cutting-edge translational... candidates to patients. PsychoGenics is seeking an Associate Director (or Director , depending on experience) who… more
    PsychoGenics (07/02/25)
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  • Associate Director , Foreign Trade Zone…

    Merck (Rahway, NJ)
    **Job Description** **Associate Director - Foreign Trade Zone** The Associate Director FTZ will be a key Trade team member within the Logistics & Regions Org. of ... our Company's Research & Development Global Clinical Supply Chain. The core responsibilities are full ownership and accountability of several FTZ's and spearheading… more
    Merck (08/29/25)
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  • Global Director , Continuous Improvement

    Catalent Pharma Solutions (Bridgewater, NJ)
    **Job Title: Global Director , Continuous Improvement** **Location: Bridgewater, NJ** **Position Summary** The focus of this role will be identifying and implementing ... plan and execute the production of commercial and late-stage clinical products efficiently, timely, and with high quality. Scope...of the cost transformation across the company. The Global Director Continuous Improvement will be part of the team… more
    Catalent Pharma Solutions (07/08/25)
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  • Senior Principal Scientist/Associate…

    Bristol Myers Squibb (Princeton, NJ)
    …facilitates the transition of drug candidates from early to late-stage clinical development, their approval and life cycle management. Early-stage translational ... the development, and maximize the potential, of BMS's therapies post- clinical proof-of-concept, including registrations and life-cycle management. Translational disease… more
    Bristol Myers Squibb (08/30/25)
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