About this role
About the Role ICON is seeking a Clinical Research Associate II based in Beijing to join its world-leading clinical research organization. You will design and analyse clinical trials, interpret complex medical data, and contribute to advancing innovative treatments. This role focuses on hands-on trial monitoring and collaboration to ensure quality, data integrity, and patient safety. What You'll Do
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborate with investigators and site staff to facilitate smooth study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports. What We're Looking For
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 2 years of experience as a Clinical Research Associate.
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
- Willingness to travel as required (approximately 60%). Nice to Have Compensation & Benefits Salary and benefits are competitive and designed to support well-being and work-life balance, including:
- Various annual leave entitlements.
- Health insurance offerings.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme LifeWorks with 24-hour access to a global network of professionals.
- Life assurance.
- Flexible country-specific optional benefits (childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others).
- ICON is committed to inclusion and belonging, providing an accessible environment for all candidates.