Phase I CRA II — CA Resident, Travel‑Heavy

Fortrea; California (MO); On-site; USD 100,000 - 120,000; Full time

Job summary

Fortrea is seeking a Clinical Research Associate with at least 1 year of clinical monitoring experience, preferably in Phase I, to support California-based trials. The role involves on-site monitoring, regulatory adherence, and coordination with vendors and study staff.

Responsibilities include ensuring proper informed consent, data integrity, and SAE reporting, with 40–50% overnight travel. The environment emphasizes fast-paced, compliant execution and teamwork across sites.

Qualifications

• 1+ year of clinical monitoring experience; Phase I experience preferred.

Responsibilities

• Monitor study sites for protocol compliance and data integrity.
• Manage site activities, perform pre-study and initiation visits, and assist with close-outs.
• Complete SAE reporting, narratives, and follow-up as required.

Skills

Clinical Monitoring

Site Monitoring

Teamwork

Regulatory Compliance

Travel Readiness

Education

University degree in allied health or nursing

Tools

EDC systems

Job description

Fortrea is seeking a Clinical Research Associate with at least 1 year of clinical monitoring experience, preferably in Phase I, to support California-based trials. The role involves on-site monitoring, regulatory adherence, and coordination with vendors and study staff.

Responsibilities include ensuring proper informed consent, data integrity, and SAE reporting, with 40–50% overnight travel. The environment emphasizes fast-paced, compliant execution and teamwork across sites.