• Parexel (Trenton, NJ)
    **Job Summary:** Parexel is seeking a Patient Recruitment & Retention Specialist to join our dynamic FSP team. This role will be key in supporting the successful ... efforts, and supporting internal and external review / approval clinical & MLR process and related documentation tracking +...study team members to file documents in the electronic Trial Master File (eTMF) for relevant projects according to… more
    DirectEmployers Association (10/10/25)
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  • Parexel (Trenton, NJ)
    …in Lupus is preferred -Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability ... experience treating rheumatology patients clinically and/or who possess extensive rheumatology clinical trial related experience will be considered for this… more
    DirectEmployers Association (10/10/25)
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  • Parexel (Trenton, NJ)
    …or Canadian equivalent + Experience as a Physician in Industry or as a clinical trial investigator is required + Previous CRO experience is strongly preferred ... value the importance of teamwork. **Knowledge And Experience** + Experience in clinical medicine (general or specialist qualifications) with Fellowship or… more
    DirectEmployers Association (10/10/25)
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  • Clinical Trial Specialist

    Actalent (Long Branch, NJ)
    Job Title: Clinical Trial Specialist As a Clinical Trial Specialist , you will coordinate the initiation and activation of all new clinical ... is essential. Responsibilities + Coordinate the initiation and activation of clinical trial protocols. + Verify Scientific Review Board, Institutional… more
    Actalent (10/14/25)
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  • Lead Pharmacovigilance QC Specialist

    United Therapeutics (Trenton, NJ)
    …experience in pharmacovigilance in either case processing or quality assurance of ICSRs ( clinical trial cases & post-marketing reports), OR + Master's Degree in ... experience in pharmacovigilance in either case processing or quality assurance of ICSRs ( clinical trial cases & post-marketing reports) + 3+ years of experience… more
    United Therapeutics (08/21/25)
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  • Senior Principal Regulatory Affairs…

    Bausch + Lomb (Trenton, NJ)
    …ensuring alignment with global requirements. + Provide guidance on risk assessment, clinical trial design implications, and regulatory pathways. + Support ... regulatory strategies for development programs and marketed products across CMC and clinical /non- clinical , labeling, adpromo areas. Serve as a strategic advisor… more
    Bausch + Lomb (09/06/25)
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  • Med Info Spec I-Pharm - Hybrid role in Titusville

    ThermoFisher Scientific (Princeton, NJ)
    …reference to pharamaceutical products or devices. Processes fulfillments and provides clinical trial information where appropriate. Analyzes caller's questions ... Two openings. **What will you do in this role?** As **Medical Information Specialist ** , you will have 2 main responsibilities. First, is providing medical and… more
    ThermoFisher Scientific (10/17/25)
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