Senior Clinical Research Associate, Medical Device

Senior Clinical Research Associate position overseeing orthopedic device clinical trials across the Midwest and West regions. The role involves monitoring sites for protocol adherence, conducting assessments, and guiding staff to maintain regulatory compliance and trial quality standards.

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 other CRAs to maintain high standards of trial conduct
• Build and maintain effective relationships with site personnel and stakeholders

Requirements

• Bachelor's degree in scientific or healthcare-related field
• 3-5 years CRA monitoring experience in CRO or pharma settings
• Strong capability managing complex protocols independently
• Proven ability to manage multiple sites and projects simultaneously
• Expertise in monitoring practices, data integrity, and clinical trial software
• Excellent communication and stakeholder management skills
• Willingness to travel approximately 60% as required

Compensation: $110,520.00-$138,150.00