Clinical Research Assistant

Job Description

• Assist with clinical research patient visits under ICH-GCP guidelines and IRB-approved study protocols or manuals of procedures.
• Coordinate subject visits, prepare study documentation, obtain written informed consent, and support patient care and subject flow.
• Collect, record, and transcribe clinical trial data, including demographics, medical history, adverse events, concomitant medications, and electronic case report forms.
• Perform protocol-required ECGs, ocular exam scribing, intraocular pressure checks, refraction, ETDRS visual acuity testing, questionnaires, and biological sample processing/shipment.
• Requires a bachelor's degree or 4 years of ophthalmic experience in lieu of a degree; no experience is required with a bachelor's degree, otherwise at least 4 years of ophthalmic experience. On-site in The Woodlands, TX; full-time, $19.00/hr plus overtime eligibility.