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Clinical Document Manager Company Name: BioBridges, LLC Due to increase in volume of work, we need another hand to support the TMF. This is a 4 month contract at the client site. The Clinical Document Manager is responsible for the structure, maintenance and control of clinical Trial Master Files (TMFs) that are required to document the conduct of clinical trials. o Clinical Document Manager is responsible for Trial Master File (TMF) quality for sponsor and/or CRO studies and serves as the primary point of contact for. 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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