Clinical Research Associate
ICON · Blue Bell
The apply link worked recently (not employer-confirmed).
Role summary
This Clinical Research Associate role involves monitoring early-development clinical trials, including site qualification, initiation, and close-out activities. The position requires ensuring protocol compliance, data integrity, and patient safety while collaborating with investigators. Candidates need a bachelor's degree in a scientific field, minimum 2 years of CRA experience, strong knowledge of ICH-GCP guidelines, and willingness to travel approximately 60%.
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 environment
- Willingness to travel approximately 60%
- Phase I experience highly preferred
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
- 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.