Senior CRA II – Medical Device Trials Lead

Fortrea; Oregon; Hybrid; USD 130,000 - 133,000; Full time

Job summary

Fortrea’s FSP team seeks an experienced Senior CRA II based in the Central region with 1+ year device experience and at least 3+ years of monitoring. The Senior CRA I will assist with project plans, lead designate projects, and may act as Local Project Coordinator.

Extensive travel is required as part of site monitoring and management across clinical studies. Responsibilities include site initiation, monitoring, data review, and regulatory compliance, with involvement in protocol development and

Qualifications

• University or college degree (life science preferred) or related allied health certification.
• Thorough knowledge of regulatory requirements and drug development processes.
• Fluent in English, both written and verbal.

Responsibilities

• Monitor and manage clinical site activities from initiation to closeout.
• Lead monitoring plans and trip report reviews for designated protocols.
• Coordinate with vendors and internal teams to ensure study timelines and budgets.
• Ensure SAE reporting, data verification, and QC reviews per SOPs.
• Support training and development of junior staff and co-monitoring.
• Travel as required (60–80% overnight).

Skills

Clinical monitoring

Site management

Regulatory knowledge

Project leadership

Travel readiness

Education

Life sciences degree

Healthcare certification

Job description

Fortrea’s FSP team seeks an experienced Senior CRA II based in the Central region with 1+ year device experience and at least 3+ years of monitoring. The Senior CRA I will assist with project plans, lead designate projects, and may act as Local Project Coordinator.

Extensive travel is required as part of site monitoring and management across clinical studies. Responsibilities include site initiation, monitoring, data review, and regulatory compliance, with involvement in protocol development and