We are seeking a detail-oriented and collaborative Clinical Research Coordinator in Denver, CO. You will drive study operations, maintain protocol compliance, and manage active trial execution across a dynamic clinical caseload. Location & Schedule: Fully On-Site (Denver, CO) | Monday – Friday 8:30 am-5:00 pmResponsibilitiesManage an active workload of 4 to 6 assigned ophthalmology and retina clinical trials simultaneously, overseeing day-to-day study execution and protocol adherence throughout the active life of enrolling trials. Conduct and oversee 10 to 15 patient visits per week, including administering detailed informed consent documentation. Partner closely with a multidisciplinary team, including unmasked/masked coordinators, 2 dedicated research assistants, and an EDC data coordinator. Work directly with practice physicians on phase-appropriate investigational drug and pharma-sponsored trials. Track and submit Adverse Events (AEs), Serious Adverse Events (SAEs), and protocol deviations in accordance with regulatory requirements.
Required Skills:
2+ years of clinical research experience 2+ years of experience in ophthalmology research. High School Diploma (minimum requirement).GCP and IATA certifications (or willingness to complete during your first week).Ability to work 100% on-site 5 days a week in Denver, CO.
