Clinical Research Associate Cross Therapeutic

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.

Responsibilities

• 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

Requirements

• 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

Compensation: $91,336-$114,170 base