Research Coordinator Training

Clinical research trials are conducted in a variety of settings by a principal investigator (PI), typically a physician. A clinical research coordinator (CRC) manages the study participants and conducts the study according to protocols and procedures. The CRC is responsible, first and foremost, for the safety and health of the study participants. Additional responsibilities include data collection, documentation and following regulatory guidelines.

Education and Training

• Many Clinical Research Coordinators receive their training and education through an Associate in Applied Science Degree in Clinical Research Coordination. The degree is a two-year undergraduate program. Students take courses that include pharmacology, regulatory compliance, and lab skills. Another form of training for CRCs is a Clinical Research Certificate. The certificate requires less than a year of study and is available online. Some CRCs hold degrees from four-year undergraduate programs and receive mostly on-the-job training.

Professional Experience and Certification

• A large part of a CRC's training is conducted at the research site. Experienced CRCs help train and oversee a new CRC on specific research protocols and procedures. Once CRCs have gained sufficient experience, they may obtain further certification through either the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA).

Continuing Professional Training

• In order to maintain certification obtained through the Association of Clinical Research Professionals and the Society of Clinical Research Associates, a CRC must have continuing education credits. The certification must be renewed every two years. More information is available from the Association of Clinical Research Professionals and the Society of Clinical Research Associates (see Resources).