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Clinical Quality Consultant - Review eTMF for completed PK study to assure all relevant documents are included. - Review study deviations to assure robust investigation performed with evaluation of impact on study. - Evaluate CRO and study site personnel training. - Review SIV and monitoring reports to determine issues and trends. - Review study changes/ document updates (protocol, pharmacy manual, lab manual, etc) to determine potential IC update and reportability to IRB. - Review IRB communications for adequacy and. After registering you may be able to apply for this job directly (if still active) on ((None))'s site. Future job matches may be sent from Geebo approved job partners.
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