Study Start Up Associate I/ II
ICON · Taipei, Taiwan
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Role summary
This hybrid role supports clinical trial operations in Taipei, managing site documentation, compliance, and logistics across assigned studies. The position requires a life sciences or healthcare background with clinical research experience, strong organizational skills, and knowledge of GCP requirements. Responsibilities include coordinating site activities, maintaining trial metrics, and mentoring junior staff.
What they're looking for
- Bachelor's degree in life sciences, healthcare, business, or equivalent clinical research experience
- Prior site support, clinical administration, or CRO/pharma healthcare experience
- Knowledge of clinical trial processes, GCP, and site documentation requirements
- Strong organizational and problem-solving abilities managing multiple priorities
- Excellent communication and interpersonal skills with service-oriented approach
- Independent work capability with effective cross-functional collaboration
What you'll be doing
- Coordinate site document collection, review, and maintenance with accuracy and compliance
- Serve as operational liaison addressing site staff questions on documentation and processes
- Track and update site status, metrics, and milestones in clinical trial management systems
- Support logistics and planning for site meetings, investigator meetings, and monitoring visits
- Mentor junior Site Specialists and identify workflow improvement opportunities
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.