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Clinical Research coordinator

EyeSouth Partners - Gainesville, FL

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Job Description

Company Overview Join Vitreo Retinal Associates! At Vitreo Retinal Associates, we're more than a leading retina specialty practice-we're a team dedicated to preserving and restoring vision for our patients. Specializing in advanced care for retinal conditions like macular degeneration, diabetic retinopathy, and retinal detachment, we combine cutting-edge technology with compassionate, personalized treatment. Our culture is built on collaboration, innovation, and continuous learning. We value every team member's contribution and provide opportunities for professional growth in a supportive environment. With multiple locations across North Florida, we're proud to serve our community and make a meaningful impact every day. If you're passionate about excellence in patient care and want to be part of a team that truly makes a difference, we invite you to join us! Vitreo Retinal Associates is affiliated with EyeSouth Partners' premier network of medical and surgical specialty eye care services. Position Summary We are now hiring for a Clinical Research coordinator that will support a high-volume Research Department within an ophthalmic practice that focuses on providing quality and compassionate care to each patient needing complete eye care services. Responsibilities A CRA is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols. • Recruit and screen subjects to participate in trials • Coordinate patient visits and perform procedures related to research • Collect accurate data obtained from research visits • Monitor research participants to ensure adherence to study protocol • Adhere to Good Clinical Practice (GCP) guidelines including regulatory and ethical standards • Maintain relationships with site staff, study subjects, and sponsor delegates • Perform other related duties as assigned by the Clinical Research Coordinator • Maintain compliance with all research Standard Operating Procedures (SOPs) Qualifications Education and/or Work Experience Requirements: • 2+ years in healthcare, preferably ophthalmology, but not necessarily in clinical research • Analytical mindset • Attention to detail • Exceptional interpersonal skills • Superior verbal and written communication skills • Understanding of laboratory procedures and equipment • Proficiency in MS Office - Word, Excel and Outlook • High school diploma or equivalent GED Company Benefits We offer a competitive benefits package to our employees: • Medical • Dental • Vision • 401k w/ Match • HSA/FSA • Telemedicine (100% company paid) • EAP (100% company paid) • Group Life/AD&D (100% company paid) • STD (100% company paid) • LTD (100% company paid) • Generous PTO Package • 7.5 Paid Holidays • Flexible Scheduling • Employee Discounts and Perks We are an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. #IND

Created: 2026-03-04

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