• Head of Biospecimen Management

    Sanofi Group (Morristown, NJ)
    …antibodies) of clinical trials, focusing on biospecimen operations. + Reviewing clinical trial protocols and Informed Consent Forms to ensure that the ... that are collected for pharmacokinetic, immunogenicity, or biomarker analyses in Sanofi's clinical trials. Main Responsibilities: + Leads a global team that supports… more
    Sanofi Group (06/13/25)
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  • Principal Database Developer

    Cytel (Trenton, NJ)
    …designing scalable and compliant data systems, and ensuring seamless integration across clinical trial phases. You are passionate about innovation, thrive in ... where talent, experience, and integrity come together to advance the state of clinical development. **Who Are You?** We are seeking a highly experienced and… more
    Cytel (08/14/25)
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  • Director, R&D Data Science & Digital Health, RWE…

    J&J Family of Companies (Titusville, NJ)
    …real-world data sources (EHR, insurance claims, registry data); familiarity with clinical trial data structure + Excellent interpersonal, communication and ... + Provide thought leadership to generate actionable insights from historical trial data, observational databases, and literature reviews to support regulatory agency… more
    J&J Family of Companies (07/19/25)
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  • US Medical Director, RSV Franchise - Vaccines

    Sanofi Group (Morristown, NJ)
    …guidance to internal Sanofi customers, including contribution of medical information and clinical trial data for pharmacovigilance (PV) and regulatory reports to ... + Provide external scientific education on disease states, epidemiology, and clinical trials of franchise product(s), support company positions, and provide guidance… more
    Sanofi Group (08/13/25)
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  • Global Publications Lead for Oncology…

    Belcan (Whippany, NJ)
    …in interpreting data and developing publications *Proven ability to interpret scientific and clinical trial data and derive scientific themes from the findings ... tactical plan that will ensure comprehensive dissemination of the preclinical and clinical data to medical, scientific professionals and patients involved in the… more
    Belcan (08/27/25)
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  • Director, Patient Reported Outcomes

    J&J Family of Companies (Raritan, NJ)
    …statisticians prior to database lock. The PRO Director helps to interpret the PRO clinical trial results. The PRO Director helps to prepare relevant sections of ... compounds and disease areas. In collaboration with the compound development and clinical teams, as well as commercial functions, the PRO Director develops the… more
    J&J Family of Companies (08/22/25)
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  • Senior Medical Science Liaison, Dermatology (North…

    J&J Family of Companies (New Brunswick, NJ)
    …and act as liaison to R&D, Medical Affairs and operations teams + Provides clinical trial support to identify potential sites, resolve issues with enrolled ... and business needs. The Sr. MSL is considered an established scientific and clinical knowledge lead on current and future J&J Innovative Medicine products per… more
    J&J Family of Companies (08/12/25)
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  • Senior Manager, Statistical Programming

    Regeneron Pharmaceuticals (Warren, NJ)
    …or related field with 9+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related ... leadership and contributes to the programming support for processing data from clinical studies. Project requirements will be identified according to a Statistical… more
    Regeneron Pharmaceuticals (07/31/25)
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  • Associate Director, DSCS Digital Implementation…

    Merck (Rahway, NJ)
    …**Valid Driving License:** **Hazardous Material(s):** **Required Skills:** Budget Development, Business, Clinical Supply Chain Management, Clinical Trial ... DSCS Digital Implementation Project Manager** Within the Development Sciences and Clinical Supply (DSCS) organization, the Digital Project Manager will streamline… more
    Merck (07/19/25)
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  • Associate Director, Global Regulator Strategy,…

    Bristol Myers Squibb (Princeton, NJ)
    …DSURs, etc. + Co-lead the cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol amendments ... plans. + Provide strategic regulatory input to key development documents, including clinical protocols, clinical and nonclinical reports and summary documents,… more
    Bristol Myers Squibb (08/30/25)
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