Senior CRA, Medical Device

Senior Clinical Research Associate position at ICON overseeing medical device clinical trials with focus on protocol adherence, regulatory compliance, and site management. Reports to sponsor-dedicated team supporting orthopedic device development.

Responsibilities

• Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
• Conduct site visits to assess performance, resolve issues, and provide operational support
• Collaborate with cross-functional teams on timely and accurate data collection and reporting
• Train site staff and coordinate with other CRAs to maintain clinical trial conduct standards
• Build and maintain relationships with site personnel and stakeholders

Requirements

• Bachelor's degree in scientific or healthcare-related discipline
• 3-5 years clinical research associate monitoring experience in CRO or pharma
• Strong ability to manage complex protocols independently and guide others
• Proficiency with clinical trial software and data integrity practices
• Excellent communication and stakeholder management skills
• Willingness to travel approximately 60% including limited Canadian travel
• Medical device or orthopedic/sports medicine experience preferred

Compensation: $110,520–$138,150 base