Clinical Research Monitoring (CRA)

Retina Consultants of Texas

Schertz, TXFull-timePosted Apr 26, 2026

Behavioral Health Market Context

Latest national behavioral health workforce report (2026-W21)Texas behavioral health workforce newsBrowse all behavioral health workforce news
Apply Nowvia Jooble

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)
Apply for this Position

More Jobs