Clinical Trial Associate
ICON · Taipei, Taiwan
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
ICON seeks a Clinical Trial Associate to support clinical trial coordination, documentation management, and regulatory compliance. The role involves assisting with trial design analysis, maintaining study files, and collaborating across teams to ensure protocol adherence and successful trial execution.
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 abilities
- Ability to work collaboratively with attention to detail in fast-paced settings
- Legal right to work in Taiwan
What you'll be doing
- Coordinate and administer clinical trials while ensuring protocol and regulatory compliance
- Maintain and organize clinical trial documentation, study files, and regulatory submissions
- Support preparation of study materials including informed consent and case report forms
- Facilitate cross-functional team communication for smooth trial execution
- Track and report clinical trial metrics and milestone progress
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.