Phase CRA II Driven Site Monitoring Impact
Listed on 2026-09-30
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Science
Clinical Research, Research Assistant/Associate
Fortrea is seeking a Clinical Research Associate to monitor Phase I trials with 1+ years of experience. The role involves site visits, adherence to protocol, data integrity, and SAE reporting across sites in the Kansas/Midwest region.
The candidate will conduct initiation and close-out visits, manage study files, and work closely with vendors. Travel up to 50% is expected, with opportunities to contribute to training and local project coordination.
This posting is for the Phase I CRA II — Travel-Driven Site Monitoring Impact role at Fortrea, based in KS, United States.
We would love to welcome a new Phase I CRA II — Travel-Driven Site Monitoring Impact to our team in KS, United States.
For the Phase I CRA II — Travel-Driven Site Monitoring Impact position at Fortrea, we are reviewing applications now.
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