CRA 2
ICON · Kuala Lumpur, Malaysia
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Associate II responsible for monitoring clinical trials, ensuring protocol compliance and data integrity. The role involves site management activities, data review, and cross-functional collaboration to support study conduct and advance innovative treatments.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years of Clinical Research Associate experience
- 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 fast-paced environments
- Willingness to travel approximately 60% as required
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 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 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.