Senior Medical Device CRA II: Site Lead & Monitoring

Fortrea; Austin (TX); On-site; USD 130,000 - 133,000; Full time

Job summary

Fortrea’s FSP team is seeking an experienced Central-based Senior CRA II with 1+ year of device trial experience and at least 3 years of monitoring experience. The role focuses on site monitoring, management, and leading project activities, with travel as an essential function.

Responsibilities include site visits, protocol adherence, data quality reviews, and collaboration with vendors and sponsors. Strong regulatory knowledge and effective communication are required.

Qualifications

• Three or more years of clinical monitoring experience.
• Advanced site monitoring and site management skills.
• Experience with Serious Adverse Event (SAE) reporting and narratives.
• Valid driver’s license and ability to travel 60–80%.

Responsibilities

• Monitor and manage clinical study sites, including routine monitoring and closeout.
• Lead monitoring plans and trip report reviews for assigned protocols.
• Coordinate with sponsor, vendors and internal teams to ensure protocol adherence.
• Contribute to protocol development and CRF review as assigned.
• Ensure regulatory compliance and audit readiness at sites.

Skills

Clinical Monitoring

Site Management

Registry Administration

Travel Coordination

MS Office

Driver's License

SAE Reporting

Team Mentoring

Education

Life science degree

Tools

MS Office

Job description

Fortrea’s FSP team is seeking an experienced Central-based Senior CRA II with 1+ year of device trial experience and at least 3 years of monitoring experience. The role focuses on site monitoring, management, and leading project activities, with travel as an essential function.

Responsibilities include site visits, protocol adherence, data quality reviews, and collaboration with vendors and sponsors. Strong regulatory knowledge and effective communication are required.