• Clinical Research Associate

    IQVIA (Durham, NC)
    …prior monitoring experience. * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
    IQVIA (10/18/25)
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  • Clinical Research Associate

    IQVIA (Durham, NC)
    **Position Summary** The Clinical Research Associate (CRA) will be responsible for designing, planning, coordinating, and conducting all activities involved ... Skills and Knowledge Requirements** + ≥2 years of experience as a Clinical Research Associate , with specific in vitro diagnostics study experience +… more
    IQVIA (11/05/25)
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  • Clinical Research Associate

    IQVIA (Durham, NC)
    …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
    IQVIA (09/03/25)
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  • Associate / Medical Director - Rheumatology…

    Parexel (Raleigh, NC)
    …Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to travel 15-20% is required _**Internal ... expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global...of the projects according to contracted agreement with the sponsor (ie: tasks and time per task contracted) and… more
    Parexel (10/11/25)
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  • CRA 2, Early Clinical Development, IQVIA…

    IQVIA (Durham, NC)
    …candidates located East, Central or West Coast. **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a ... expectations. Your work will directly contribute to the integrity and quality of clinical research data. **Key Responsibilities** + Conduct all types of site… more
    IQVIA (11/01/25)
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  • Associate Director, Client Services

    IQVIA (Durham, NC)
    …IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates ... ** Associate Director, Client Services - Clinical ...mid-size environment is highly preferred. + Experience in the Clinical Research industry is highly preferred. +… more
    IQVIA (10/31/25)
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  • Associate Medical Director/Medical Director…

    ThermoFisher Scientific (Greenville, NC)
    …management and oversight of all contracted services. **Discover Impactful Work:** The Associate /Medical Director provides medical oversight of clinical trials to ... with the applicant's training (comparable to 2 years); Or + Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company… more
    ThermoFisher Scientific (10/09/25)
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  • Sr. Grant Budget Specialist

    Actalent (Raleigh, NC)
    …a research -related field. + Two years of experience in grant or clinical research , budget development, billing compliance, research contract management, ... in accordance with regulations and policies. + Provide interpretation assistance of research funding opportunities and ensure compliance with sponsor and… more
    Actalent (11/07/25)
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  • GLOBAL Project Manager (FSP), Remote (US)

    ThermoFisher Scientific (Wilmington, NC)
    …Sciences preferred.** **Skills:** **Knowledge in global regulatory and compliance requirements for clinical research , including but not limited to US CFR, EU ... (oral and written)** **Experience:** **5+ years' experience in pharmaceutical industry and/or clinical research organization, including 3+ years clinical more
    ThermoFisher Scientific (11/06/25)
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  • Project Manager (FSP), Remote (US)

    ThermoFisher Scientific (Greenville, NC)
    …and preparations **Skills:** + Knowledge in global regulatory and compliance requirements for clinical research , including but not limited to US CFR, EU CTD, ... (oral and written) **Experience: 6+ years' experience in pharmaceutical industry and/or clinical research organization, including 4+ years clinical study… more
    ThermoFisher Scientific (09/27/25)
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