As a Clinical Research Coordinator, a team member will be involved in an array of activities as listed below: Serve as primary contact for research protocols at affiliated hospitals Direct the conduct of clinical studies to ensure adherence to the research protocol Conduct screening, recruitment, counseling and follow-up of study subjects Participate in initiation visits, investigator s meetings, monitoring visits and close-out visits for assigned clinical trials and implement these trials according to a deadline schedule mutually agreed upon by PI and sponsor/CRO Participate in Informed Consent Process & Documentation Perform relevant submissions to IRB/IEC Report SAEs to the sponsor/CRO and the IRB/IEC Prepare, update & maintain Site File and patient records Ensure accurate and complete data entry into case report forms or pre-established computer programmed formats ensuring appropriate source documentation Advise & alert investigators of potential protocol and regulatory violations Ensure audit readiness of site