Trish Landry

Biography

With more than 20 years’ experience navigating regulatory processes and managing clinical trials, Trish oversees all aspects of Beaufort’s clinical operations and helps clients implement clinical programs and regulatory affairs strategies. She coordinates domestic and international clinical trial programs, focusing on protocol development, data collection and management, CRA training and management, investigator selection, recruitment and training, site initiations, periodic monitoring and close-outs as well as clinical study report preparation. She also has extensive experience in the preparation of multiple U.S. regulatory submissions and has effectively led FDA GCP and QSR inspections. With more than 20 years’ experience navigating regulatory processes and managing clinical trials, Trish oversees all aspects of Beaufort’s clinical operations and helps clients implement clinical programs and regulatory affairs strategies. She coordinates domestic and international clinical trial programs, focusing on protocol development, data collection and management, CRA training and management, investigator selection, recruitment and training, site initiations, periodic monitoring and close-outs as well as clinical study report preparation. She also has extensive experience in the preparation of multiple U.S. regulatory submissions and has effectively led FDA GCP and QSR inspections.

Research Interest

Medical Science