Remote Phase I Clinical Research Associate II

Fortrea; San Diego (CA); On-site; USD 100,000 - 120,000; Full time

Job summary

Fortrea is seeking a Clinical Research Associate with 1+ years of clinical monitoring experience, preferably with Phase I trials, to join our California team. The role includes site monitoring, data integrity checks, SAE processing, and collaboration with vendors and staff.

Ideal candidates reside in California, with the ability to travel overnight 40-50%. Strong clinical judgment, regulatory understanding, and teamwork are essential for success in this fast-paced environment.

Qualifications

• 1+ years of Clinical Monitoring experience.
• Phase I experience preferred.
• Willingness to travel 40-50% overnight.

Responsibilities

• Monitor clinical sites: routine visits, close-out, and maintenance of study files.
• Ensure protocol and regulatory compliance; obtain informed consent.
• Assist with SAE reporting and data query resolution.
• Coordinate Local Project Coordinator tasks and client contacts.
• Support training of new staff and co-monitoring activities.

Skills

Clinical Monitoring

Phase I experience

Travel readiness

Education

University or college degree or related certification

Job description

Fortrea is seeking a Clinical Research Associate with 1+ years of clinical monitoring experience, preferably with Phase I trials, to join our California team. The role includes site monitoring, data integrity checks, SAE processing, and collaboration with vendors and staff.

Ideal candidates reside in California, with the ability to travel overnight 40-50%. Strong clinical judgment, regulatory understanding, and teamwork are essential for success in this fast-paced environment.