Job Description

The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI).  While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. 

Essential Duties and Responsibilities:

Assisting trial Investigator in screening and review of potential study participants eligibility

Maintaining case report forms, charts and documentation

Mentoring, training, and high-level oversight of other clinical research coordinators and research assistants

Ensuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements

Collecting and entering data as necessary

Assist management with potential new hire selection and shadowing process

Assist with study start-up, maintenance, and close-out of studies as needed for those on the team

Ability to be flexible with study assignments