A Clinical Trials Coordinator Professional (CRCPro) course is a program that trains clinical research coordinators (CRCs) to facilitate, supervise, and support clinical trials in accordance with good clinical practice (GCP) standards, and also prepares you for the certification exam offered by the Biopharma Institute.
The CRCPro course covers topics such as: ICH-GCP Good Clinical Practice Clinical Trials: Preparing for an Audit or Inspection ICH E6 (R2) GCP Training for Investigator Site Personnel Overview of ICH E8 (R1): General Considerations for Clinical Studies Guideline Good Documentation Practices and ALCOA-C HIPAA Training for Clinical Trial Professionals.