Site Specialist II
ICON · Tokyo, Japan +1 more
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
The Site Specialist II will manage site-level documentation, compliance, and operational coordination across assigned clinical trial sites. Responsibilities include document collection and review, serving as a liaison for site staff, maintaining trial management systems, coordinating meetings and monitoring visits, and supporting process improvements. The role requires a bachelor's degree in life sciences or healthcare, clinical research experience, knowledge of GCP and trial processes, and strong organizational and communication skills.
Privacy & handoff
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