Clinical Research Associate
ICON · US
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Clinical research associate needed to conduct site qualification, monitoring, and close-out activities for multi-therapeutic and oncology trials. Responsibilities include ensuring protocol compliance, maintaining data integrity, and collaborating with investigators. Requires a scientific bachelor's degree, minimum 9 months CRA monitoring experience, ICH-GCP knowledge, and ability to travel 60% domestically and internationally.
Where this listing comes from
This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-05 (originally posted 2026-08-20). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.
Privacy & handoff
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