About this role
Job title: Clinical Research Associate II
About the Role As a Clinical Research Associate II at ICON Beijing, you will contribute to design, monitoring and analysis of clinical trials, ensuring data integrity and patient safety. You will work with investigators and site staff to support high-quality study conduct and regulatory compliance.
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 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%).
Compensation & Benefits
- Competitive salary and a range of additional benefits designed to support well-being and work-life balance.
- Various annual leave entitlements.
- Health insurance offerings, retirement planning, LifeWorks 24-hour global assistance, life assurance.
- Flexible country-specific optional benefits including childcare vouchers, bike purchase schemes, gym memberships, subsidized travel passes, health assessments, among others.
- ICON is committed to inclusion and equal opportunity for all candidates.