Assuming the role of Study Manager, you will be responsible to successfully carry out the following responsibilities: * Conduct clinical studies; participating in writing study protocols, amendments, and administrative changes based on the approved synopsis * If applicable, participate in selection of all vendors for assigned studies; provide oversight of vendors including communicating expectations, timelines, planning content for study meetings * Oversee the monitoring of investigational sites ...
CareerTopJobs.com - 3 years ago
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