Clinical Trial Associate
ICON · Beijing, China
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Trial Associate position supporting the design, coordination, and administration of clinical trials. The role involves maintaining trial documentation, ensuring regulatory compliance, and collaborating with cross-functional teams to advance innovative treatments.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Prior experience or demonstrated interest in clinical research
- Knowledge of clinical trial processes, regulations, and guidelines
- Excellent organizational and communication skills
- Ability to work collaboratively with attention to detail
- Willingness to travel approximately 10% as required
What you'll be doing
- Coordinate and administer clinical trials while ensuring protocol and regulatory compliance
- Maintain and organize clinical trial documentation including study files and regulatory submissions
- Support preparation of study materials such as informed consent forms and case report forms
- Facilitate communication across cross-functional teams to ensure trial execution
- Track and report clinical trial metrics and milestones
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.