Remote CRA 2: Clinical Trial Monitoring Pro

Fortrea; Pennsylvania; Hybrid; USD 100,000 - 112,000; Full time

Job summary

Fortrea is seeking a CRA 2 in the United States (Ohio, Pennsylvania, or Virginia) with at least 2 years of monitoring experience. Expect 8–10 on-site days per month, with a mix of onsite and remote work.

The role focuses on site monitoring, data integrity, SAE handling, and coordination of local projects. The candidate should have a university degree or allied health certification and be comfortable with frequent travel and fast-paced, team-oriented environments.

Qualifications

• 2 years of Clinical Monitoring experience.
• Overnight travel expected (60% travel).

Responsibilities

• Monitor clinical sites including routine monitoring and close-out visits.
• Maintain study files and initiate visits; liaise with vendors.
• Ensure staff have materials and instructions to enroll patients.
• Verify informed consent procedures and protocol compliance.
• Ensure data integrity on CRFs and data tools.
• Perform SAE reporting and follow-up.
• CRF review and data query resolution.
• Assist with training of new employees and local project coordination.
• Coordinate designated projects as Local Project Coordinator.

Skills

Overnight travel

Clinical Monitoring

Education

University degree or allied health certification

Job description

Fortrea is seeking a CRA 2 in the United States (Ohio, Pennsylvania, or Virginia) with at least 2 years of monitoring experience. Expect 8–10 on-site days per month, with a mix of onsite and remote work.

The role focuses on site monitoring, data integrity, SAE handling, and coordination of local projects. The candidate should have a university degree or allied health certification and be comfortable with frequent travel and fast-paced, team-oriented environments.