Clinical Research Technician
Listed on 2026-01-27
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Healthcare
Healthcare Nursing
Overview
Clinical Research Technician role at Retina Consultants of Texas (RCTX). This position combines ophthalmic technical skills with research administration to provide clinical support and education about complex clinical trials while maintaining patient flow and communication within a high-volume practice. The technician works exclusively within the EMR system (Nextech) supporting providers as they interact with patients. Travel to multiple clinics and variable hours (Monday – Friday, 6:30 am – 6:30 pm) may be required.
Weekend hours are possible if available.
RCTX is an Equal Employment Opportunity and Affirmative Action Employer and is committed to creating an inclusive work environment that celebrates diversity. RCTX follows CDC and local protocols to ensure safety for patients, providers, employees, and communities.
Responsibilities- Clinical Functions:
Obtain comprehensive patient history (chief complaint, history of present illness, family history of ocular and general illnesses, allergies, current medications) and document accordingly. - Accurately perform and document visual acuity, confrontation visual fields, evaluation of motility, pupillary function tests, dilation, and ocular tonometry.
- Assist physicians with laser procedures, injections, and minor procedures while maintaining sterile and safe environment protocols.
- Perform intraocular pressure checks after injections.
- Provide compassionate patient care throughout the clinic flow and maintain cleanliness in exam and procedure rooms; manage supply stock.
- Counsel, consent, set up, and assist with in-office procedures.
- Research Functions:
Counsel and educate patients regarding clinical trials, articulating complex study information clearly. - Conduct informed consent processes for research studies.
- Administer all mandatory questionnaires to study subjects.
- Prepare visit-specific documentation and charts for the Physician Clinic Team.
- Promptly request all necessary medical records for Serious Adverse Event Reporting.
- Process and ship laboratory biological samples for analysis.
- Coordinate and schedule subject visits within study windows per protocol and guidelines.
- Transcribe subject study information from source documents to Electronic Case Report Forms.
- Obtain applicable sponsor training and/or certifications.
- Performs other duties as assigned.
- High school diploma required
- Bachelor of Science in Biology preferred
- Previous healthcare or research experience preferred but not required
- Ability to understand and articulate complex concepts
- Quick learning ability and adaptability
- Bilingual capabilities preferred (English primary)
- Demonstrates hard work and dedication
- Exhibits authentic care for patients and colleagues
- Shows innovation and problem-solving abilities
- Must be able to walk and stand for the duration of the shift
- Move frequently between exam rooms; assist with patient transfers
- Type or write legibly in a dimly-lit setting
- Hear softly spoken words
- Assist elderly patients getting in and out of exam chairs
- Lifting up to 30 pounds
- Entry level
- Full-time
- Research, Analyst, and Information Technology
- Medical Practices
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