Clinical Research Monitoring (CRA)

Retina Consultants of Texas

Schertz, TXFull-timePosted Apr 26, 2026

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Benefits

In addition to being highly challenged professionally, the following competitive benefits are provided for full‒time eligible employees 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 (Roth and Traditional, starting date of hire)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, 8 paid holidays + 1 floating holiday annuallyStarting Pay Rate: $19.00 per hour, eligible for overtime1 more items(s)

Qualifications

  • •Ability to multitask
  • •Computer efficient
  • •Communicates well both verbally and electronically; email, MS Teams, etc
  • •Bachelor’s degree or 4 years of ophthalmic experience in lieu of degree
  • •No experience required with a Bachelor’s degree; otherwise at least 4 years of ophthalmic experience
  • •2 more items(s)

Responsibilities

  • •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
  • •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
  • •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 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
  • •16 more items(s)
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