Sarah Cannon Research Institute (SCRI) is seeking a Clinical Project Associate to ensure the Trial Master File is set up and maintained in audit-ready condition. You will manage TMF/eTMF document collection and perform quality reviews throughout the trial lifecycle.
Role involves coordinating with investigators, sites, and cross-functional teams to ensure timely delivery of study documents and regulatory compliance.
#J-18808-LjbffrRemote TMF Quality Assurance Associate in workfromhome at Unknown Company
This position is listed as full time and onsite.