CRA II
ICON · Kuala Lumpur, Malaysia
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Associate II role based in Kuala Lumpur, responsible for monitoring clinical trials including site qualification, initiation, and closeout activities. The position requires managing protocol compliance, data integrity, and patient safety while collaborating with investigators. Candidates need a scientific degree, minimum two years of CRA experience, ICH-GCP knowledge, and willingness to travel approximately 60%.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years clinical research associate experience
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP guidelines
- Strong organizational and communication skills with attention to detail
- Ability to work independently and collaboratively in fast-paced environment
- Willingness to travel approximately 60%
- Legal right to work in Malaysia
What you'll be doing
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure protocol compliance, data integrity, and patient safety
- Collaborate with investigators and site staff on study conduct
- Review data and resolve queries to maintain clinical data quality
- Prepare and review 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.