Clinical Research Coordinator

Implement and complete clinical research protocols by obtaining informed consent, training team members, and performing study tasks per written protocols. Collaborate with the Research Financial Analyst to ensure accurate billing while conducting clinical trials that involve human subjects in adherence to Good Clinical Practice (GCP) Guidelines. Create valid source documentation, maintain records of patient visits, and monitor adverse events for reporting to the sponsor. Recruit and screen potential subjects, respond to data queries, and maintain biannual or triannual research certification. Schedule is Monday through Friday, 8am to 5pm, with some flexibility. Travel is required.