• Research Support Specialist (A)

    University of Miami (Miami, FL)
    …research data related to assigned research studies. Works closely with the faculty investigator and the primary investigator in the implementation of daily study ... meetings with the assistance of the faculty investigators and principal investigator . Implements day-to-day project activities including the preparation of research… more
    University of Miami (04/29/25)
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  • Executive Medical Director, Product Safety…

    BeOne Medicines (San Mateo, CA)
    …and review of study specific medical monitoring plans + Participates in investigator meetings, as needed, accountable for product safety profile and reviews, ... updates of safety presentation content **Developmental Product Safety Monitoring and Surveillance : (Protocol** **Specific)** + Accountable for the analysis of SAEs… more
    BeOne Medicines (04/26/25)
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  • Medical Director, Global Medical Affairs,…

    J&J Family of Companies (Raritan, NJ)
    …evidence generation and dissemination strategies for company sponsored and investigator -initiated studies (IIS), including registries. + Have a leadership role ... for the development of materials to be used for clinical study execution ( investigator brochures, training materials, etc.). + Work closely with Medical Safety team… more
    J&J Family of Companies (05/23/25)
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  • Medical Director, Medical Affairs, Johnson…

    J&J Family of Companies (Cincinnati, OH)
    …procedural evidence generation and dissemination strategies for company sponsored and investigator initiated research, including registries. + Have a leadership role ... oversight for the development of materials to be used for study execution ( investigator brochures, training materials, etc.). + Work closely with Medical Safety team… more
    J&J Family of Companies (05/22/25)
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  • Open Rank Medical Director of the Adult Diabetes…

    University of Colorado (Aurora, CO)
    …Medicine's criteria for Associate Professor. + Strong track record as Principal Investigator for clinical research grants (industry or non-profits like NIH, JDRF, ... for full Professor. + Strong track record as Principal Investigator for clinical research grants (industry or non-profits like...be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you… more
    University of Colorado (05/20/25)
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  • Clinical Sciences Professional (Open Rank…

    University of Colorado (Aurora, CO)
    …all studies the team manages + Collaborating with and supporting the principal investigator and lab manager with research functions + Ability to follow protocols and ... and their offspring. In our group, we study both investigator and industry-initiated human subject trials. The lab is...be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you… more
    University of Colorado (04/30/25)
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  • Principal Clinical Science Professional

    University of Colorado (Aurora, CO)
    …deviations, creating source documents, creating backup plans, and ensuring principal investigator oversight. + Assist with identifying issues related to operational ... + Communicate and collaborate with various colleagues (eg, principal investigator , clinicians, medical staff, sponsors, contract research organizations (CROs), other… more
    University of Colorado (04/04/25)
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  • Open Rank Laboratory Sciences Professional…

    University of Colorado (Aurora, CO)
    …team members on laboratory protocols and operations. + May assist the principal investigator with the development and writing of research protocols. + May assist the ... Principal Investigator with the development and writing of manuscripts and...be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you… more
    University of Colorado (03/09/25)
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  • Executive Director, Clinical Development (MD)…

    Gilead Sciences, Inc. (Santa Monica, CA)
    …may include, but are not limited to, additional study or investigator documentation, contributions to data analysis plans, study reporting, and clinical ... limited to assessment of eligibility criteria, toxicity management, and drug safety surveillance . + Leads or otherwise oversees and directs the clinical development… more
    Gilead Sciences, Inc. (05/20/25)
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  • Associate Medical Director, Pharmacovigilance…

    Sumitomo Pharma (Raleigh, NC)
    …assessment for assigned investigational and marketed products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing ... Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports (CSR), Investigator 's Brochures (IB), Investigator communications (Dear Health Care Provider… more
    Sumitomo Pharma (05/16/25)
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