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Research Protocol Specialist 2 - 21839Mayo Clinic - Rochester, MNThe Research Protocol Specialist II assists in the development and maintenance of the protocol document and process from initial receipt of participation through study completion, termination and/or publication. Responsibilities may include, but are not limited to: preparing drafts of Mayo Informed Consent Forms (ICFs), determining appropriate forms and documentation for Institutional Review Board (IRB) submission, such as participating modalities, investigational drug brochures, investigational new drug (IND) approvals, regulatory materials and draft addenda where appropriate. Position provides input to amendments and submits protocol modifications to the IRB within specified timeframe. Position independently determines changes necessary to forms and writes/distributes communications due to...originally from MinnesotaJobNetwork.com - More Tools...
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