As clinical research expands within the optometry field, the research coordinator’s role is gaining long-overdue recognition. These professionals make research feasible and compliant in everyday eye care settings. Whether you’re an optometrist seeking to diversify your services or a professional exploring a new career path, understanding the function and value of the research coordinator can open doors to innovation and impact.

Clinical trials are no longer reserved for academic centers or large institutions. With proper planning and training, they can be successfully integrated into everyday optometric practice. The research coordinator plays a vital role in organizing logistics, managing compliance, and protecting patients—ultimately helping advance the field of eye care.

A research coordinator manages all components of a clinical study: patient recruitment, data collection, documentation, and communication with sponsors. This individual ensures that everything from patient visits to regulatory reporting is done accurately and on time. It’s a dynamic position that requires both clinical insight and operational discipline.

The ideal coordinator is organized, meticulous, and adaptable. Strong communication skills are essential, as coordinators must often explain study protocols to patients, interact with doctors, and handle inquiries from sponsors. Equally important is the ability to multitask and handle unexpected disruptions calmly.

A research coordinator may handle fundus photography, IOP measurements, or advanced imaging, depending on the study. Being comfortable with various clinical tools is a plus.

Most research coordinators begin with Good Clinical Practice (GCP) training and International Council for Harmonisation (ICH) guidelines certification. These are often sponsored by study sponsors or available online for free or at low cost. A helpful resource is the Clinical Research Coordinator Handbook, which provides an overview of acronyms, workflows, and regulatory responsibilities.

Additionally, mentorship and on-the-job experience are often key. Many coordinators, like Amy Bland, entered the field after working in ophthalmology or optometry clinics and discovering a passion for research through exposure and encouragement.

To integrate clinical research into your optometry practice, begin with three foundational steps:

Research can run like a “practice within a practice,” complementing patient care without interrupting your clinical flow.

Each clinical trial has its own cadence. Some studies last months, others years. Coordinators must plan how many patients to enroll, how long each visit will take, and how testing fits into the existing practice schedule. Post-visit documentation often takes as long as the clinical appointment itself.

Sponsors perform regular monitoring visits to ensure protocol adherence and verify data. Coordinators manage these interactions and must promptly address any “queries” related to errors or inconsistencies in documentation.

No matter how organized a team is, protocol deviations happen. Missed windows, patient cancellations, and misread instructions are common, especially early in a study. That’s why dry runs and single-subject test cases are strongly encouraged before full launch.

From ethical consent to backup treatment options, research protocols are designed to ensure that patient safety and clinical standards remain paramount.

Research coordinators are the operational backbone of clinical trials. For optometrists and ophthalmologists, partnering with a strong coordinator opens new opportunities for growth, visibility, and early access to the latest therapies. For professionals stepping into the coordinator role, the path offers autonomy, purpose, and continuous learning.

Bold Takeaway: The research coordinator is the keystone of clinical trial success in eye care—bridging practice and progress.

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