Clinical Research Coordinator

Seeking a Clinical Research Coordinator in Modesto, CA** Join a nationally recognized leader in retina care and clinical research! We are a growing private medical practice specializing in the diagnosis and treatment of diseases of the retina and vitreous. Our physicians are nationally recognized, and we remain at the forefront of retina care by utilizing advanced technology and actively participating in -and designing - innovative clinical trials that help advance treatment options for patients with retinal diseases. With 250+ team members, we offer a fast-paced, collaborative environment where healthcare professionals can build their careers, expand their clinical research expertise, and work alongside highly respected physicians and research professionals. We are seeking a full-time Clinical Research Coordinator to join our clinical research department. The Clinical Research Coordinator will be responsible for coordinating clinical research visits and ensuring studies are conducted in accordance with ICH-GCP guidelines, IRB requirements, and study protocols. This is an excellent opportunity for a research professional who enjoys working directly with patients, physicians, clinical teams, and pharmaceutical sponsors and is interested in developing expertise within ophthalmology and retina research. Coordinate day-to-day clinical trial activities and patient research visits. Review and understand study protocols, timelines, inclusion/exclusion criteria, and study-specific procedures. Screen and recruit potential research participants and support enrollment goals. Perform protocol-specific clinical research procedures, which may include scribing, visual field testing, VFQ questionnaires, IOP measurements, and other study assessments. Enter and maintain clinical trial data in electronic data capture (EDC) systems and resolve data queries within required timelines. Identify, document, and report adverse events (AEs), serious adverse events (SAEs), and other required safety information. Maintain regulatory documentation, including protocols, investigator brochures, IRB documentation, CVs, training records, and investigator disclosures. Ensure study staff training is completed and appropriately documented. Coordinate sponsor/CRO monitoring visits and assist with site visit preparation and follow-up. Work collaboratively with physicians, research staff, clinical teams, business office staff, and pharmaceutical sponsor representatives. Participate in investigator meetings, study teleconferences, and other research-related activities as needed. Ensure clinical trials are conducted accurately, efficiently, and in compliance with applicable regulations and protocols. High school diploma or equivalent. ~2+ years of clinical research experience OR CRCC/CCRP certification. ~ Experience in ophthalmology or retina clinical research. Experience with ophthalmic equipment and/or clinical trial procedures. Ability to write and document accurately. Ability to communicate effectively by telephone. Manual dexterity to operate ophthalmic equipment. Full-Time Employee Benefits: ~7 paid holidays annually. ~ Medical insurance, with the employer paying 95% of the premium for the base HMO plan for employees . Dental, vision, life, and accident insurance options. Flexible Spending Account (FSA) options for eligible medical, dental, vision, and dependent-care expenses. Join a team that is helping shape the future of retina care and clinical research . You'll have the opportunity to work alongside nationally recognized physicians, gain hands-on experience with innovative clinical trials, and make a meaningful impact on patients living with retinal diseases.