Clinical Research Coordinator II - Richmond, VA

Coordinate daily clinical trial activities across GI and hepatology therapies; lead patient recruitment by chart reviews, protocol discussions with patients, and consent verification to meet enrollment targets; schedule patient visits and procedures per protocol; conduct patient visits and dispense study medication, perform ECGs and blood draws; ensure data entry into CTMS and maintain study files (consent forms, source docs, CRFs, investigational accountability); maintain data quality and timely documentation; act as point of contact for participants; adhere to SOPs and GCP; communicate with CRO, sponsor, PI, and site team; support data verification and monitor preparation; require 3+ years of clinical research and IBD experience; phlebotomy experience preferred; strong written and verbal communication; ability to read and apply clinic policies and protocols; lifting up to 25 pounds; accommodations available upon request.