Phase CRA II Driven Site Monitoring Impact
Listed on 2026-10-30
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Research/Development
Clinical Research, Research Scientist, Research Assistant/Associate, Regulatory Compliance Specialist
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.
Are you ready to take on the Phase I CRA II — Travel-Driven Site Monitoring Impact role at Fortrea?
The position is based in KS, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 100..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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