Clinical Research Assistant

Retina Consultants of Texas (RCTX) is seeking a Research Assistant to join our innovative team with the mission of Fighting Blindness For The World To See. This position will be responsible for assisting in research patient visits according to ICH‑GCP guidelines and the IRB‑approved study protocol. Day‑to‑day activities may include all or some of the essential functions listed below, depending upon individual experience, knowledge, and the needs of the organization which are subject to change from time to time. The role is based at our Schertz Clinic and requires support of the Research Department hours of 6:30 am‑5 pm Monday through Friday. Benefits In addition to being highly challenged professionally, full‑time eligible employees receive a competitive benefits package after a 60‑day introductory period: Employee‑Paid Benefits: Medical, Dental, Vision, short‑term disability, voluntary life insurance, accident, critical illness, hospital indemnity, pet insurance, HSA pre‑taxed contributions, 401(k) retirement savings contributions (Roth and Traditional). Employer‑Paid Benefits: Long‑term disability, $25,000 basic life insurance policy, 3% 401(k) safe harbor contribution, HSA employer contributions, annual performance merit increases, certification opportunities, rewards & recognition platform, WellHub Starter Plan Gym Membership, paid time off and (8) paid holidays + (1) floating holiday annually. Starting Pay Rate: $19.00 per hour, eligible for overtime. Responsibilities Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines. Prepare visit‑specific documentation and charts for the Clinical Research Coordinator. Inform subjects and obtain written consent regarding ICFs. Assist Coordinator in patient care and management. Assist Coordinator in monitoring subject flow and subject care. Accurately collect and record all necessary data (demographics, medical history, adverse events, concomitant medications, etc.) during study visits. Transcribe subject study information from source documents to the Electronic Case Report Forms. Administer all mandatory questionnaires to study subjects. Set up, prepare subject, and conduct electrocardiograms on subjects who require ECG per study protocol. Scribe ocular exams for doctors and confirm appropriate treatment per protocol. Promptly request all necessary medical records for Serious Adverse Event Reporting. Collection, processing, and shipment of laboratory biological samples for analysis. Perform intraocular pressure checks post‑injections. Review and resolve data management queries as needed. Trial frame refraction and ETDRS visual acuity testing. Other duties as assigned. Qualifications Bilingual preferred. Ability to multitask. Computer efficient. Communicates well both verbally and electronically via email, MS Teams, etc. Detail oriented. Education Requirements Bachelor’s degree or 4 years of ophthalmic experience in lieu of degree. Experience Requirements No experience required if you have a bachelor’s degree; otherwise at least 4 years of ophthalmic experience. RCTX is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, age, national origin, disability, military service, veteran status, genetic information, or any other protected class under applicable law. #J-18808-Ljbffr The Michaels Organization