Hybrid Clinical Study Monitor: IRB & Compliance
Listed on 2026-10-10
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Healthcare
Clinical Research
UTMB Health is seeking a Clinical Study Monitor to oversee administrative and regulatory aspects of clinical research across IRB-approved studies. This hybrid role focuses on safety, data integrity, and compliance with US CFR, ICH, and GCP guidelines.
The position requires a strong background in clinical research, collaboration with investigators, and ability to coordinate monitoring visits and prepare reports for regulatory review.
We are looking to fill the Hybrid Clinical Study Monitor: IRB & Compliance position at Utmb in Galveston, TX, United States.
All applications are reviewed carefully by our team.
The position is based in Galveston, TX, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 70..
We aim to respond to suitable candidates as soon as possible.
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