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SENIOR CLINICAL SCIENTIST Management of the operational components of clinical trials for PhI-IIa studies in support of global regulatory filings including IND, NDA, MAA and life-cycle management programs. CO-author complex protocols with minimal direction. Able to interpret relevance of review comments and incorporate as appropriate. Ensure protocol specific content and BMS required sections are included in the Informed Consent Form. Interacts and manages stakeholder expectations with functional groups outside of. 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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