Clinical Research Associate - Cross Therapeutic Area

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.

Responsibilities

• 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

Requirements

• 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

Compensation: $91,336.00-$114,170.00