Clinical Site Associate
ICON · Beijing, China
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
ICON seeks a Clinical Site Associate to support clinical trial site management activities in Beijing. The role involves coordinating site activation, maintaining documentation systems, facilitating communications between sites and project teams, and ensuring compliance with regulatory standards.
What they're looking for
- Bachelor's degree in life sciences, healthcare, business, or related field
- Preferred experience in clinical research, administration, or regulated environments
- Strong organizational skills managing multiple tasks and deadlines
- High attention to detail in documentation and data entry
- Proficiency with MS Office and electronic systems/databases
- Effective written and verbal communication skills
What you'll be doing
- Support site activation including document collection, review, and tracking of approvals
- Maintain current site information and status in clinical trial management systems
- Assist CRAs with site communications, follow-up, and resolution of queries
- Coordinate logistics for site visits, meetings, and documentation preparation
- Ensure accurate filing and maintenance of essential documents for audit readiness
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.