• Director - Quality Control

    Catalent Pharma Solutions (Madison, WI)
    …service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience ... testing products, raw materials, and the manufacturing environment to ensure the safety , quality, identity, purity, and potency produced by the Catalent Madison… more
    Catalent Pharma Solutions (08/08/25)
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  • Clinical Research Coordinator, On-Site, Horsham,…

    IQVIA (Horsham, PA)
    …Functions** + Coordinate clinical research studies conducted by a supervising principle investigator . + May assist as back-up CRC on other studies + Develops ... maintains source documentation + Manages inventory and administers test articles/investigational product to participants + Performs data entry and query resolution +… more
    IQVIA (10/15/25)
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  • Global Senior Director Medical Affairs (GDMA),…

    Merck (North Wales, PA)
    …and advisory boards + Serves as the medical representative within Product Development sub-teams (including Clinical, V&I, Commercial, Publications, and Label), ... data generation study concepts and protocols when requested. + Reviews Investigator -Initiated Study proposals from key countries prior to headquarters submission… more
    Merck (10/07/25)
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  • VP, Medical Science and Strategy…

    ThermoFisher Scientific (Greenville, NC)
    …issues + Drug class issues + Protocol and indication considerations, including safety + Team education on indication + Interactions with clients physicians and ... Through PPD's consulting practice, the incumbent will provide Industry gold standard product development plans, and top-level design of clinical trial protocols that… more
    ThermoFisher Scientific (10/05/25)
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  • Vice President, Medical Science and Strategy…

    ThermoFisher Scientific (Frederick, MD)
    …issues + Drug class issues + Protocol and indication considerations, including safety + Team education on indication + Interactions with clients physicians and ... Through PPD's consulting practice, the incumbent will provide Industry gold standard product development plans, and top-level design of clinical trial protocols that… more
    ThermoFisher Scientific (10/05/25)
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  • Associate Scientist, Biology- Discovery

    Merck (De Soto, KS)
    …upon assignment by the supervisor. The incumbent will act as study investigator /supervisor or responsible scientist to organize, conduct and report routine animal ... Scientist will fulfill general tasks within the organization related to safety , compliance, and laboratory maintenance, and will interact closely with fellow… more
    Merck (10/04/25)
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  • Senior Clinical Scientist - Job ID: SCS

    Ascendis Pharma (Palo Alto, CA)
    …Ensure successful completion of documents (including clinical trial protocols, investigator brochures, monitoring plans, site training materials, clinical study ... across multiple endocrine projects + Ensure study integrity, and track accumulating safety and efficacy data + Anticipate obstacles within a clinical trial, and… more
    Ascendis Pharma (10/03/25)
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  • Director, Clinical Development

    Intra-Cellular Therapies, Inc (Bedminster, NJ)
    …Bedminster, NJ. Founded on Nobel-prize winning research, we launched our first commercial product in CNS in 2020 and received approval for an expanded indication in ... 3. Act as primary contact for medical communication to ensure medical safety within studies. Develop and maintain relationships with sites and Investigators. 4.… more
    Intra-Cellular Therapies, Inc (09/29/25)
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  • US Medical Director - Rhino - Gastro

    Sanofi Group (Cambridge, MA)
    …based in Morristown, NJ or Cambridge, MA. The role functions internally as the product expert to lead the development and execution of the most efficient and ... objectives. + Reviewing and approving medical and scientific content of Regulatory, Safety , Scientific Affairs, Medical Affairs, and Commercial. + Ensuring that all… more
    Sanofi Group (09/23/25)
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  • Principal Clinical Scientist

    Abbott (Maple Grove, MN)
    …planning for products and process changes, to gain regulatory approval for product release, additional claims or indications, by addressing issues from a clinical, ... teams and lead the execution of the publication strategy through coordination with investigator authors and internal teams. + Serve as an active member of study… more
    Abbott (09/17/25)
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