• Senior Clinical Research Director, I&I

    Sanofi Group (Bridgewater, NJ)
    …and shares relevant information within and beyond Project teams + Provide medical expertise to the clinical studies (except select Exploratory Pharmacology studies) ... Support other clinical development activities (eg pressure test and cluster feasibility, medical review and validation of clinical data, study risk assessment) +… more
    Sanofi Group (04/06/25)
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  • Associate Director, Laboratory Data Management

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …in a medical device, pharmaceutical company, or similar environment (eg, CRO ); oncology, immunology, or complex disease Strong knowledge of Clinical trial data ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
    Daiichi Sankyo Inc. (05/14/25)
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  • Trial Supplies Manager

    System One (Trenton, NJ)
    …Affiliates, Medical Affairs (MA), Regulatory, CMC, QA, Packaging Vendors, CRO 's, IRT Organizations, and Global Clinical Supply Chain Functional Operations to ... plan and protocol analysis. * Reviewing and providing input for draft medical protocols to develop packaging and labelling configurations and create packaging… more
    System One (05/30/25)
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  • Director, Global Clinical Development

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …markets innovative products, with a focus on pharmaceutical products to meet unmet medical needs and nutraceutical products for the maintenance of everyday health We ... protocols. + Develop focused expertise to serve as a clinical/ medical scientific consultant to health economic, medical ...value. + Provide strategic oversight in our vendor and CRO relationships and provide clinical input into their governance… more
    Otsuka America Pharmaceutical Inc. (04/17/25)
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  • Senior Clinical Scientist, Immunology

    Bristol Myers Squibb (Princeton, NJ)
    …activities as applicable + Evaluate innovative trial designs (collaboration with Medical Monitor/Clinical Development Lead) + Protocol and ICF development process ... of cross functional comments and ensuring high clinical quality (collaboration with Medical Writing) + Site-facing activities such as training and serving as primary… more
    Bristol Myers Squibb (05/21/25)
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  • Director, Global Clinical Development-Rheumatology…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …designs and protocols. + Develops focused expertise to serve as an clinical/ medical scientific consultant to health economic, medical affairs, marketing, ... (ie, GDCP) and oversees trials essential for determining the clinical safety, efficacy, medical usefulness and value of drug or medical device product… more
    Otsuka America Pharmaceutical Inc. (04/17/25)
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  • Senior Solution Consultant

    Norstella (Trenton, NJ)
    …leading providers of data and intelligence on clinical trials, drug treatments, medical devices and what's new in the regulatory and commercial landscape. Relying ... of the world's leading pharmaceutical, contract research organizations (CROs), medical technology, biotechnology and healthcare service providers, including the top… more
    Norstella (05/06/25)
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  • Senior Principal Engineer, Investigator…

    J&J Family of Companies (Raritan, NJ)
    …or Medical Device company or a Clinical Research Organization ( CRO ) is required. + Proficiency supporting Information Technology systems and related processes ... to participate in the following Company sponsored employee benefit programs: medical , dental, vision, life insurance, short- and long-term disability, business… more
    J&J Family of Companies (05/17/25)
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  • Director, Clinical Pharmacology Lead

    Organon & Co. (Jersey City, NJ)
    …(biostatistics, clinical operations) and external (contract research organization [ CRO ], bioanalytical and/or modeling vendors) colleagues. The Clinical Pharmacology ... early development plans. The Clinical Pharmacology Lead will serve as the medical monitor and/or study director responsible for the execution (in conjunction with… more
    Organon & Co. (04/29/25)
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  • Senior Study Manager

    Actalent (Morristown, NJ)
    …profiles, final protocols, and amendments. + Coordinate document review and medical writing tasks, including ICF, CRF guidelines, IB, and safety communications. ... + Oversee the CRO and vendor selection process, including the creation of...for this temporary role may include the following: * Medical , dental & vision * Critical Illness, Accident, and… more
    Actalent (05/31/25)
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