Senior CRA II - Medical Device Trials Lead

Fortrea; Oklahoma City (OK); On-site; USD 130,000 - 133,000; Full time

Job summary

Fortrea is seeking a Senior CRA II to lead site monitoring and site management for central region studies. You will ensure protocol adherence, data integrity, and regulatory compliance while coordinating with sponsors and Fortrea teams.

Expect 60-80% travel, with responsibilities spanning site initiation, monitoring, and closeout, and the potential to mentor junior staff. This role offers growth within a dynamic CRO environment.

Qualifications

• Three years of clinical monitoring experience required.
• Thorough understanding of regulatory requirements and drug development process.
• Fluency in local language and English, both written and verbal.

Responsibilities

• Monitor and manage clinical study sites, including pre-study visits and closeouts.
• Lead site monitoring activities and contribute to monitoring plans.
• Prepare trip reports and manage project tasks under supervision.
• Coordinate with vendors and handle regulatory submissions as needed.
• Review data quality and ensure SAE reporting and documentation compliance.
• Train and supervise junior staff and act as local project coordinator when assigned.

Skills

Clinical Monitoring

Site Management

Project Coordination

Regulatory Knowledge

SOP Compliance

Travel Coordination

SAE Reporting

Team Leadership

Communication Skills

Education

Bachelor's degree in Life Sciences

Certification in allied health

Nursing certification

Medical or laboratory technology background

Job description

Fortrea is seeking a Senior CRA II to lead site monitoring and site management for central region studies. You will ensure protocol adherence, data integrity, and regulatory compliance while coordinating with sponsors and Fortrea teams.

Expect 60-80% travel, with responsibilities spanning site initiation, monitoring, and closeout, and the potential to mentor junior staff. This role offers growth within a dynamic CRO environment.