Clinical Study Specialist
ICON · Warren, NJ +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 hybrid role supports clinical trial operations across multiple sites, handling administrative coordination, documentation management, and regulatory compliance tasks. Responsibilities include organizing study reports, scheduling meetings, maintaining trial records, and tracking site activation and enrollment progress. The position requires a bachelor's degree and at least two years of clinical research experience.
Privacy & handoff
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