Clinical Research Associate Program + GCP Certificate - CRI001

Clinical Research is one of nation’s most vital undertakings, leading to improved medical care, new preventive methods and improved quality of life for patients.  Every year, pharmaceutical companies spend billions of dollars in developing drugs that go through rigorous trials and checks before being introduced in the market. Clinical research professionals play a vital role in the drug development process by conducting, monitoring clinical trials and managing clinical trials within good clinical practice (GCP) guidelines and regulations.  It is widely recognized, however, that the efficiency and effectiveness of clinical research professionals depend on strong understanding of regulations and policies that pertain to the conduct and oversight of clinical trials.

The goal of Clinical Research Associate program offered by Clinwell is to develop and train professionals to understand and navigate an array of regulations and policies that pertain to conducting, monitoring and managing clinical trials. The program covers various aspects of a clinical trial from site selection, patient recruitment, choice of the investigator, study conduct, protocols, safety documentations, and study close out.  In addition, the program is designed to cover international regulations. Our students learn from some of the best faculty in the industry who are certified practitioners with deep experience in clinical trials and monitoring and have a wide knowledge of ICH-GCP, GMP, GLP and HIPAA.