About this role
Job title: IVD CRA, Shanghai
About the Role ICON is seeking an IVD Clinical Research Associate (CRA) in Shanghai to oversee and coordinate clinical trials, ensure regulatory compliance, and collect/analyze trial data. This role involves on-site activities with travel and a focus on patient safety and data integrity.
What You'll Do
- Work independently to set up and monitor a study, complete accurate status reports, and maintain study documentation
- Run sponsor-generated queries efficiently and manage study cost efficiency
- Participate in the preparation and review of study documentation and feasibility studies for new proposals
- Develop and maintain collaborative relationships with investigators, site staff, and stakeholders
- Ensure patient safety by adhering to ICON procedures, protocols, and regulatory requirements
What We're Looking For
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines and ability to review/evaluate medical data
- Excellent written and verbal English communication
- Strong interpersonal skills to handle queries promptly
- Ability to travel at least 60% (international and domestic); valid driver's license
Compensation & Benefits
- Competitive salary and a range of benefits
- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme LifeWorks (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 equal opportunity