• Associate Medical Director, PVRM

    Sumitomo Pharma (Topeka, KS)
    …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 (08/02/25)
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  • Director, Clinical Operations

    Bausch + Lomb (Topeka, KS)
    …updates on progress and changes in scope, schedule, and resources. + Organize investigator and expert meetings relevant to the indication and assist with the ... provide clinical operations support and guidance for the ongoing surveillance of the safety of patients in clinical trials...handled by the CRAs and responded to by the site/ investigator in a timely manner. May assist in the… more
    Bausch + Lomb (06/07/25)
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