The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-
day operations of clinical trials, recruiting and screening study participants, as well as documenting

and reporting on the daily operations of assigned trials. Working in collaboration with the Principal
Investigator, the Sr. CRC is responsible for the oversight, facilitation and coordination of the daily
clinical trial activities and plays a critical role in the conduct of the study. The Sr. CRC works
collaboratively with the entire team, sponsors, and Clinical Quality Associates to ensure productivity,
quality, and timely completion of studies.
The Sr. CRC is expected to support, guide, train, demonstrate and lead clinical trial team members in
the implementation of trial related activities. The Sr. CRC applies critical thinking and creative
problem-solving skills across a wide variety of clinical studies, and contributes to the development of
new processes, procedures, tools and training to enhance clinical research activities and is
accountable for adhering to quality standards.