Clinical Research Associate II
ICON · FL +1 more
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
This role involves serving as a primary liaison between clinical trial sites and sponsors in oncology studies, conducting site visits, monitoring compliance with regulations and protocols, and managing patient safety reporting. The position requires a Bachelor's degree in life sciences or nursing credentials, at least two years of on-site monitoring experience, and proficiency in clinical systems; up to 50% travel across the southeast region is expected.
Privacy & handoff
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