Job Description

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 pm

Responsibilities

• Manage 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.

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