• Summer 2026 - Clinical Research and Development…

    Bristol Myers Squibb (Madison, NJ)
    …+ Reviews literature and prepares summary documents for inclusion in Investigator Brochure, protocols, regulatory submission documents, etc. + Assists Clinical ... process, direct your inquiries to ###@bms.com . Visit careers.bms.com/ (https://careers.bms.com/ eeo -accessibility) eeo -accessibility to access our complete Equal… more
    Bristol Myers Squibb (10/23/25)
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  • Director, Medical Strategy, Global Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …with Medical Evidence Generation (MEG) to oversee the execution of the Investigator Sponsored Research (ISR) programs from concept through full execution, including ... process, direct your inquiries to ###@bms.com . Visit careers.bms.com/ (https://careers.bms.com/ eeo -accessibility) eeo -accessibility to access our complete Equal… more
    Bristol Myers Squibb (10/22/25)
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  • Associate Clinical Project Management Director,…

    IQVIA (Parsippany, NJ)
    …and deliver trial-specific training materials. + Coordinate and participate in Investigator Meetings. **Budget & Financial Oversight** + Establish country budgets ... customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled more
    IQVIA (10/22/25)
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  • (Senior) Clinical Research Associate - Sponsor…

    IQVIA (Parsippany, NJ)
    …are available for filing in the Trial Master File (TMF) and verify that the Investigator 's Site File (ISF) is maintained in accordance with GCP / ICH and local ... customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled more
    IQVIA (10/13/25)
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  • Principal Medical Writer - FSP

    Parexel (Trenton, NJ)
    …for a wide range of documents, including but not limited to investigator 's brochures, clinical study protocols and reports, integrated summaries, literature reviews, ... documents **Education:** + BA/BS, Advanced degree preferred \#LI-LO1 \#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants… more
    Parexel (10/11/25)
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  • Principal Medical Writer- FSP

    Parexel (Trenton, NJ)
    …for a wide range of documents, including but not limited to investigator 's brochures, clinical study protocols and reports, integrated summaries, literature reviews, ... in a wide range of disciplines Education: * BA/BS or higher \#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive… more
    Parexel (10/11/25)
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  • Director, MEG Lead Immunology & Neuroscience,…

    Bristol Myers Squibb (Madison, NJ)
    …Collaborations (CRCs), Medical Affairs Sponsored Studies (MAST), and Investigator -Sponsored Research Studies (ISRs), ensuring alignment with internal strategies ... process, direct your inquiries to ###@bms.com . Visit careers.bms.com/ (https://careers.bms.com/ eeo -accessibility) eeo -accessibility to access our complete Equal… more
    Bristol Myers Squibb (10/10/25)
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  • Senior Manager, Clinical Data Management

    Bristol Myers Squibb (Princeton, NJ)
    …(BLA)/Market Authorization Application (MAA)] **Travel Required:** 5-10% Industry Conferences, Investigator Meetings, Regulatory Inspections (as needed) If you come ... process, direct your inquiries to ###@bms.com . Visit careers.bms.com/ (https://careers.bms.com/ eeo -accessibility) eeo -accessibility to access our complete Equal… more
    Bristol Myers Squibb (10/10/25)
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  • Spring 2026 Co-Op Early Clinical Development…

    Bristol Myers Squibb (Princeton, NJ)
    …of clinical study protocols and related documents (eg, Informed Consent Forms, Investigator Brochures). + Support the design and implementation of clinical trials in ... process, direct your inquiries to ###@bms.com . Visit careers.bms.com/ (https://careers.bms.com/ eeo -accessibility) eeo -accessibility to access our complete Equal… more
    Bristol Myers Squibb (10/04/25)
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  • CRA 2, Car-T, Iqvia Biotech

    IQVIA (Parsippany, NJ)
    …collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards. + Document site management ... customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled more
    IQVIA (10/02/25)
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