Clinical Research Assistant

7 days ago


Conroe Texas, United States Retina Consultants of Texas Full time
Job Summary

We are seeking a highly detail-oriented and organized Clinical Research Assistant to join our team at Retina Consultants of Texas. As a key member of our research team, you will be responsible for coordinating and scheduling subject visits, preparing documentation, and collecting and recording data.

Responsibilities
  • Coordinate and schedule subject visits within study-specific windows per protocol guidelines.
  • Prepare visit-specific documentation and charts for Clinical Research Coordinator.
  • Inform subjects and obtain written consent in regard to ICFs.
  • Assist Coordinator in patient care and management.
  • Accurately collect and record all necessary data during study visits.
  • Transcribe subject study information from source documents to Electronic Case Report Forms.
  • Administer 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.
Requirements
  • Bilingual preferred.
  • Ability to multitask.
  • Computer efficiency.
  • Effective communication skills, both verbally and electronically.
  • Detail-oriented.
  • 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.


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