• Investigator Senior

    Elevance Health (Middletown, NY)
    ** Investigator Senior ** **Supports the Payment Integrity line of business** _Location: This position will work a hybrid model (remote and office)._ _Alternate ... determined to recover, eliminate and prevent unnecessary medical-expense spending. The ** Investigator Senior ** is responsible for the independent identification,… more
    Elevance Health (01/22/25)
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  • Senior Clinical Research Associate (Remote)

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    **Job Description Summary** The Senior Clinical Research Associate (CRA) will act as a liaison between BD (the study Sponsor) and the sites/clinics that conduct ... compliance, the CRA will work closely with the Principal Investigator and their staff at their assigned clinical study...their staff at their assigned clinical study sites. The Senior CRA will identify and/or resolve data queries and… more
    BD (Becton, Dickinson and Company) (01/16/25)
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  • Senior Director Clinical Development…

    Teva Pharmaceuticals (Parsippany, NJ)
    Senior Director Clinical Development - Respiratory Date: Jan 21, 2025 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: ... people to make a difference with. **The opportunity** This is a new Senior Director role to support the growth within the respiratory clinical development program… more
    Teva Pharmaceuticals (01/22/25)
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  • Senior Manager, Medical Writing, Oncology

    Gilead Sciences, Inc. (Parsippany, NJ)
    …markets around the world. We have an exciting and unique opportunity for a senior level medical writer ( Senior Manager, Medical Writing, Oncology) to join our ... complexities, such as clinical study reports (CSRs all phases, investigator 's brochures, CTD summaries/overviews, PIPs/PIP modifications, and regulatory responses).… more
    Gilead Sciences, Inc. (11/18/24)
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  • ( Senior ) Clinical Research Associate…

    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 ... regulatory requirements. * Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. * Act as a… more
    IQVIA (01/16/25)
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  • Director, Clinical Operations (Oncology)

    Gilead Sciences, Inc. (Parsippany, NJ)
    …including study protocols. + Serve as a member of the Clinical Operations Oncology Senior Leaders Forum providing key input into the leadership and management of the ... Solve problems relating to national and international regulations, guidelines and investigator interactions. + May also serve as the Clinical Operations… more
    Gilead Sciences, Inc. (01/08/25)
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  • Associate Director, Medical Writing

    Gilead Sciences, Inc. (Parsippany, NJ)
    …such as clinical study reports (CSRs) (all phases), investigator 's brochures, CTD summaries/overviews, PIPs/PIP modifications, and regulatory responses. ... timelines and resource planning for assigned projects. + May serve as a senior medical writer and department representative for a large development program or TA,… more
    Gilead Sciences, Inc. (11/15/24)
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