Phase I CRA II - Travel-Heavy Trials

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

Job summary

Fortrea is seeking a Clinical Research Associate with 1+ years of experience to join our Phase I team in California. You will monitor trials, ensure regulatory compliance, and support site operations in a fast-paced environment.

Ideal candidates have Phase I experience, are willing to travel 40-50% and maintain high data integrity and subject safety. This role offers exposure to diverse trials and collaboration with cross-functional teams across Fortrea.

Qualifications

• 1+ years of Clinical Monitoring experience required.
• Phase I experience preferred.
• University or college degree or allied health certification required.

Responsibilities

• Monitor study sites including routine monitoring and close-out.
• Manage site activities per project plans and ensure data quality.
• Verify informed consent procedures and protocol adherence.
• Assist with training of new staff and coordination of local projects.

Skills

Clinical Monitoring

Phase I experience

Education

Bachelor's degree or allied health certification

Job description

Fortrea is seeking a Clinical Research Associate with 1+ years of experience to join our Phase I team in California. You will monitor trials, ensure regulatory compliance, and support site operations in a fast-paced environment.

Ideal candidates have Phase I experience, are willing to travel 40-50% and maintain high data integrity and subject safety. This role offers exposure to diverse trials and collaboration with cross-functional teams across Fortrea.