Clinical Trial Associate
On-siteBeijing, Beijing, China
Job Summary
Coordinate and administer clinical trials while ensuring compliance with protocols and regulatory requirements. Maintain and organize clinical trial documentation, including study files and regulatory submissions, and support the preparation of materials such as informed consent forms and case report forms. Work with cross-functional teams to facilitate communication and track clinical trial metrics and milestones. This role requires a Bachelor's degree in a scientific or healthcare-related field and prior experience in clinical research. Based in Beijing, ICON offers a competitive total rewards package including health coverage, retirement plans, and learning opportunities.
Required Qualifications
- Bachelor's degree in a scientific or healthcare-related field
- Prior experience or strong interest in clinical research
- Knowledge of clinical trial processes, regulations, and guidelines
- Excellent organizational and communication skills
- Ability to work collaboratively in a fast-paced environment with attention to detail
- Legal right to work in the country where the role is based
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