Clinical Research Associate - Cross Therapeutic Area
ICON · Denver, CO +1 more
Clinical OperationsFull-time$91k–$114kCompany career page
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Role summary
ICON Strategic Solutions seeks a Clinical Research Associate to serve as the primary liaison between investigational sites and sponsors in a cross-therapeutic area role based in Denver. The position involves conducting site visits, ensuring regulatory compliance, managing documentation systems, and supporting patient safety monitoring across multiple clinical trials.
What they're looking for
- Bachelor's degree in Life Sciences or equivalent; qualified RN acceptable
- 2+ years on-site monitoring experience in pharmaceutical or CRO industry
- Proficiency in ICH-GCP, CTMS, eTMF, and local regulatory requirements
- Experience monitoring across multiple therapeutic areas
- Ability to travel 60-75% for west region site visits
- U.S. work eligibility without visa sponsorship
- Strong communication, problem-solving, and collaborative skills
What you'll be doing
- Serve as primary contact between investigational sites and sponsor
- Conduct site selection, initiation, routine monitoring, and close-out visits
- Ensure site compliance with ICH-GCP, standard operating procedures, and regulations
- Monitor patient safety and coordinate timely adverse event and serious adverse event reporting
- Maintain accurate documentation in CTMS and eTMF systems; 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.