Clinical Associate
On-site · Shanghai, Shanghai, China
Job Summary
Oversee and support the execution of clinical trials with a focus on coordinating clinical activities, ensuring adherence to protocols and regulatory requirements, and maintaining data integrity. Lead site management and monitoring, collaborate with cross-functional teams to optimize processes, track trial progress, identify risks, and implement mitigation strategies. Provide guidance to clinical staff and investigators to ensure compliance with best practices and regulatory standards, and manage multiple projects with strong organizational and problem-solving skills.
Required Qualifications
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Significant experience in clinical trial management
- Strong organizational and problem-solving skills
- Excellent communication and interpersonal skills
- Detail-oriented with proactive approach to trial success
- Employment with ICON requires legal right to work in the country where the role is based
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