Phase I Senior Clinical Research Associate (Remote)

Fortrea; Durham (NC); On-site; USD 100,000 - 130,000; Full time

Job summary

Fortrea is seeking a Senior Clinical Research Associate with 3+ years of clinical monitoring experience, preferably with Phase I exposure, to support US sites. The role involves on-site monitoring, site management, data integrity checks, SAE reporting, and coordination with project teams.

Travel of 40–50% is expected, with oversight of study activities and regulatory compliance. Ideal candidates reside in the United States and are comfortable working in a fast-paced environment with evolving

Qualifications

• University or college degree or allied health certification from an accredited institution.
• 3+ years of clinical monitoring experience.
• Phase I experience required.
• 40–50% overnight travel.

Responsibilities

• Monitors study sites, conducts pre-study and initiation visits, and maintains study files.
• Manages site activities per project plans and liaises with vendors.
• Ensures proper materials and instructions for study staff to enter patients safely.
• Verifies informed consent procedures and protocol adherence per regulatory requirements.
• Cleans data by reviewing CRFs and resolving data queries.
• Supports SAE reporting and training of new staff as needed.

Skills

Clinical Monitoring

Phase I Experience

Overnight Travel

Education

University degree or allied health certification

Job description

Fortrea is seeking a Senior Clinical Research Associate with 3+ years of clinical monitoring experience, preferably with Phase I exposure, to support US sites. The role involves on-site monitoring, site management, data integrity checks, SAE reporting, and coordination with project teams.

Travel of 40–50% is expected, with oversight of study activities and regulatory compliance. Ideal candidates reside in the United States and are comfortable working in a fast-paced environment with evolving