• Manager, Clinical Trials

    Bausch + Lomb (Columbus, OH)
    …protocol development, case report form (CRF) development, IRB submissions, investigator agreements, informed consent form (ICF) development, site selection and ... communication with senior clinical trial sites regarding all logistics including contract...Trial Materials, Marketing, Regulatory, and Quality/Compliance. + Liaising between internal and external stakeholders to facilitate cooperation of others.… more
    Bausch + Lomb (11/19/25)
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