Clinical Research Associate Cross Therapeutic
ICON · Chicago, IL +1 more
Clinical OperationsFull-time$91k–$114kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Associate responsible for managing sponsor-site relationships and conducting monitoring visits across multiple therapeutic areas. Position requires 2+ years of on-site monitoring experience and involves extensive travel across the Midwest region.
What they're looking for
- Bachelor's degree in Life Sciences or equivalent, or RN qualification
- 2+ years on-site monitoring experience in pharmaceutical or CRO industry
- Proficiency in ICH-GCP, CTMS, and eTMF systems
- Experience monitoring across multiple therapeutic areas
- Eligible to work in United States without visa sponsorship
- Ability to travel 60-75% for on-site monitoring visits in Midwest
- Strong communication, problem-solving, and collaboration skills
What you'll be doing
- Serve as primary contact between investigational sites and sponsor
- Conduct site visits including selection, initiation, monitoring, and close-out
- Ensure site compliance with ICH-GCP, SOPs, and regulatory requirements
- Monitor patient safety and manage adverse event and safety reporting
- Maintain documentation in CTMS and eTMF systems and resolve data queries
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.