Clinical Research Coordinator, Ophthalmology Trials
Overview
You will own pre-screening, enrollment, and data collection for clinical research protocols at a dedicated retina research center. Working directly with PI and a collaborative team, you will coordinate study timelines, schedule visits, and maintain regulatory binders. You will also adapt procedures for quality improvement and address adverse events per protocol. This role offers hands-on experience in ophthalmology research with a focus on patient advocacy and compliance.
What You'll Do9
- 1Perform chart review and pre-screening to determine study participant eligibility
- 2Coordinate routine activities of clinical studies including data collection, maintenance, and project evaluation
- 3Plan study timelines, schedule appointments and study visits, and coordinate meeting schedules
- 4Execute moderate to complex research tests and adapt procedures for quality improvement under supervision
- 5Operate clinical research equipment following technical instructions and troubleshoot operational failures
- 6Monitor and report adverse events to the PI or supervisor, advocating for study participants and quality standards
- 7Identify, report, and help resolve protocol deviations and unanticipated occurrences
- 8Maintain study-specific regulatory binders and follow requirements of international, national, and local regulatory bodies
- 9Complete mandatory training in safety, equality, responsible conduct of research, and research competencies
Requirements8
- 11-2 years of relevant research experience required
- 2Undergraduate degree in a related field
- 3Clinical research experience in Ophthalmology is highly preferred
- 4Certified Ophthalmic Assistant or Technician (COA/COT) preferred
- 5Good Clinical Practice certification preferred
- 6Previous research publication is a plus
- 7Proficiency in office software and computer applications
- 8Strong written and verbal communication skills
Salary Insight
Salary not disclosed in listing
Location
Required Skills
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