Lead CRA - Site Monitoring & Trials Expert
Listed on 2026-11-06
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Research/Development
Research Scientist, Clinical Research, Research Assistant/Associate
Fortrea is seeking a Clinical Research Associate in the United States to monitor trials, ensure GCP compliance, and protect study subjects. You will conduct site visits, verify source data, and manage regulatory documents while coordinating with study teams.
Ideal candidates have at least 2 years of monitoring experience, strong ICH GCP knowledge, and English proficiency. Travel up to 60% of the time to sites is required.
This is an excellent role to take on the Lead CRA
- Site Monitoring & Trials Expert role at Fortrea.
Learn more about the Lead CRA
- Site Monitoring & Trials Expert role in the description above.
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