Senior CRA - Surgical Devices (Travel ~60%)

ICON; United States; On-site; USD 111,000 - 138,000; Full time

Benefits offered by this job

Competitive base salary

Performance incentives

Medical, dental, and vision coverage

Retirement plans

Life insurance

Employee wellbeing resources

Job summary

ICON Strategic Solutions seeks Senior Clinical Research Associate specializing in surgical device trials for the Central Region. You will lead on clinical trial monitoring with focus on quality and continuous improvement.

Responsibilities include monitoring sites for protocol adherence and regulatory standards, conducting visits, collaborating with cross-functional teams, and training site staff to uphold high conduct standards. Willingness to travel ~60% is required.

Qualifications

• Bachelor's degree in Life Science or related field.
• 3–5 years of CRA monitoring experience in CRO/pharma environments.
• Strong preference for at least 1 year of medical device monitoring experience.
• In-depth knowledge of FDA regulations and ICH/GCP guidelines.
• Willingness to travel as required (approximately 60%).

Responsibilities

• Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP standards.
• Conduct site visits to assess site performance, resolve issues, and support successful trial execution.
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
• Provide training and guidance to site staff and other CRAs to maintain high standards of conduct.
• Build and maintain relationships with site personnel and stakeholders for smooth trial operations.

Skills

CRA Monitoring

FDA/ICH/GCP

Verbal & Written Communication

Travel Readiness

Education

Bachelor’s degree in Life Science

Job description

ICON Strategic Solutions seeks Senior Clinical Research Associate specializing in surgical device trials for the Central Region. You will lead on clinical trial monitoring with focus on quality and continuous improvement.

Responsibilities include monitoring sites for protocol adherence and regulatory standards, conducting visits, collaborating with cross-functional teams, and training site staff to uphold high conduct standards. Willingness to travel ~60% is required.