CRA II
ICON · Singapore
The apply link worked recently (not employer-confirmed).
Role summary
This Clinical Research Associate II role involves managing clinical trial sites through qualification, initiation, monitoring, and closure activities. Responsibilities include ensuring protocol compliance, data integrity, and patient safety while collaborating with investigators and resolving data queries. The position requires a scientific degree, minimum 2 years CRA experience, strong knowledge of clinical trial regulations and ICH-GCP guidelines, and willingness to travel 60% of the time.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 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 travel 60% of the time internationally and domestically
- Valid driver's license
- Legal right to work in Singapore
What you'll be doing
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout trial process
- Collaborate with investigators and site staff to facilitate study conduct
- Perform data review and resolve queries to maintain high-quality clinical data
- Prepare and review study documentation including protocols and clinical study reports
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.