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Clinical Trials Coordinator Professional (CRCPro) Health care and Pharmaceutical

Posted by samaa ahmed Sep 4

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About

About Course

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.

Eligibilities

which requires the following: A bachelor’s degree or higher in any field. A letter of recommendation from a client or employer. A record of experience in completing relevant CRC tasks. Documents of past trainings. Between one to three years of experience working in clinical research.

Note: Eligibility requirements may vary based on the specific course or program you choose. Please refer to the detailed course brochure for more information.

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