Clinical Research Assistant

Overview 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 and/or manual of procedures. 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. This position will be based at our Katy Clinic. Candidates must be able to meet the needs of the patients and providers, and support the Research Department hours of 6:30 am–5 pm Monday through Friday. Schedules are provided weekly and are based on the provider's clinic, patient and surgery schedules. Starting Pay Rate is $19.00 per hour and eligible for overtime. Employee Paid Benefits such as Medical, Dental, and Vision, short‑term disability, voluntary life insurance, accident, critical illness, hospital indemnity, pet insurance, HSA pre‑taxed contributions, 401(k) retirement savings contributions both Roth and Traditional options starting date of hire. Employer Paid Benefits such as 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. 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. Responsibilities Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines. Prepare visit‑specific documentation and charts for Clinical Research Coordinator. Inform subjects and obtain written consent in regard to ICF’s. Assist Coordinator in patient care and management. Assist Coordinator in monitoring subject flow and assist in subject care and management. Accurately collect and record all necessary data (e.g. demographics, medical history, adverse events, concomitant medications, etc.) during study visit. 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 subject 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 Skills/Competencies: Biliginual preferred Ability to multitask Computer efficient Commnucates well both verbally and electronically; email, MS Teams, etc. Detail oriented Education Requirements Bachelors degree or 4 years of ophthalmic experience in lieu of degree Experience Requirements: No experience required with a Bachelors degree otherwise at least 4 years of ophthalmic experience #J-18808-Ljbffr Retina Consultants Houston