Clinical Trials Source Documents Specialist
Sarah Cannon Research Institute
Sarah Cannon Research Institute (SCRI) in Nashville, TN is seeking a Source Document Specialist to support the Study Coordinator in daily trial activities. You will ensure compliance with SOPs, GCP and ICH regulations, and help secure accurate source documentation for enrolled patients. Ideal candidates hold an associate degree (bachelor preferred), at least 2 years in healthcare (oncology preferred), and strong English communication. #J-18808-Ljbffr Sarah Cannon Research Institute
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