Clinical Project Associate Jobs in Tennessee

Assist with confirming the qualifications of investigators and investigative sites throughout the conduct of the clinical trial

Set-up, document collection/upload of files to the TMF/eTMF

Perform initial quality review of documents prior to upload/filing in the TMF/eTMF

Partner with document specialist to maintain the Trial Master File (TMF) in “audit ready” condition from study start to completion

Review study documents to ensure they are current, complete and accurate

It’s More Than a Career, It’s a Mission.