Senior CRA II – Medical Device Trials Lead

Fortrea; Kansas; On-site; USD 130,000 - 133,000; Full time

Job summary

Fortrea's Central based Senior CRA II is responsible for site monitoring and site management across clinical studies, with primary oversight of monitoring activities per protocol and regulatory guidelines. The role requires 3+ years of monitoring experience and 1+ year of device experience, and involves travel 60-80%.

You will lead site visits, ensure data integrity, manage trial documentation, and coordinate with the project team.

Qualifications

• University or college degree (life science preferred)
• Thorough knowledge of regulatory requirements and drug development processes
• Fluent in local office language and English, both written and verbal

Responsibilities

• Monitor and manage site monitoring activities including routine visits and closeout.
• Lead monitoring plans and trip report reviews for assigned protocols.
• Ensure data integrity through source document verification and proper CRF review.
• Coordinate with vendors and internal teams to support study timelines.

Skills

Clinical monitoring

Site management

Regulatory knowledge

Project coordination

Communication skills

Problem solving

Driver's license

Education

Bachelor's degree in life sciences

Tools

Microsoft Office

Job description

Fortrea's Central based Senior CRA II is responsible for site monitoring and site management across clinical studies, with primary oversight of monitoring activities per protocol and regulatory guidelines. The role requires 3+ years of monitoring experience and 1+ year of device experience, and involves travel 60-80%.

You will lead site visits, ensure data integrity, manage trial documentation, and coordinate with the project team.