Phase I Clinical Research Associate II - Remote/Travel

Fortrea; Durham (NC); On-site; USD 105,000 - 118,000; Full time

Job summary

Fortrea is seeking a Clinical Research Associate II with 1+ years of on-site monitoring experience to support Phase I studies. The role requires travel (40–50% overnight) and the ability to work within a fast-paced, regulated environment in the United States.

You will monitor study sites, manage visits, ensure proper consent and protocol adherence, review CRFs, generate data queries, and assist training of new staff. Candidates with Phase I experience are preferred.

Qualifications

• University or college degree or related allied health certification.
• 1+ years of clinical monitoring experience.
• Phase I experience preferred.
• Willingness to travel 40-50% overnight.

Responsibilities

• Monitor study sites including routine monitoring, close-out visits, and maintenance of study files.
• Coordinate site management as prescribed in project plans and liaise with vendors.
• Ensure informed consent procedures and protocol adherence.
• Review CRFs and generate data queries with resolution.
• Assist with training of new staff and coordinate local projects.

Skills

Clinical Monitoring

Phase I

Travel

Education

Bachelor's degree

Tools

EDC systems

Job description

Fortrea is seeking a Clinical Research Associate II with 1+ years of on-site monitoring experience to support Phase I studies. The role requires travel (40–50% overnight) and the ability to work within a fast-paced, regulated environment in the United States.

You will monitor study sites, manage visits, ensure proper consent and protocol adherence, review CRFs, generate data queries, and assist training of new staff. Candidates with Phase I experience are preferred.