Clinical Research Coordinator (CRC) – Foundations
16 Contact Hours - 4 Days
Overview This training provides clinical research professionals with basic knowledge tailored to the CRC’s fundamental role in the conduct of clinical trials. It is designed for new CRCs and can be used by organizations as onboarding training.
Objectives
Objectives
At the end of the training, participants will:
- Understand the CRC’s critical role in the conduct of clinical trials
- Understand the concepts of participant safety, product development and regulation, clinical trial operations, study and site management, data management and informatics