Investigative Coordinator

Are you a new principle investigator or research
coordinator trying to figure this all out?

Over the last decade, IMARC has worked with many sites that were eager to get involved in clinical research. However, they did not fully appreciate the regulatory framework within which they would be required to work. The huge amount of work and knowledge required to successfully run a research study at your site can be overwhelming at best. Whether you are beginning a sponsored research study, or an investigator-initiated study, IMARC can help guide you through the complex regulatory maze with GCP training tailored specifically for your site, followed by periodic monitoring and/or auditing visits to ensure appropriate implementation.

For more information regarding training, monitoring, or auditing please contact John E. Lehmann at 440.801.1540.