Clinical Research Associate II — Remote/Hybrid Trials

Fortrea; Durham (NC); Hybrid; USD 100,000 - 112,000; Full time

Job summary

Fortrea seeks a CRO CRA 2 to support clinical monitoring in California or Colorado. The role mixes onsite and remote work with 8-10 days on site per month and up to 60% travel. A 2-year monitoring track and related degree are required.

You will monitor sites, ensure protocol compliance, manage CRFs, and coordinate with vendors and study teams across multiple sites. The position emphasizes data quality and regulatory adherence in a fast-paced environment.

Qualifications

• 2 years of Clinical Monitoring experience.
• 60% overnight travel.

Responsibilities

• Monitor all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits.
• Liaise with vendors and other duties as assigned.
• General On-Site Monitoring and ensure protocol staff have proper materials to enter patients into the study.
• Verify informed consent procedures and protocol requirements per regulatory standards.
• Ensure data integrity on CRFs and other data collection tools by monitoring source documents.
• Manage registry activities and perform feasibility work when requested.

Skills

Clinical Monitoring

Education

University degree or nursing licensure

Job description

Fortrea seeks a CRO CRA 2 to support clinical monitoring in California or Colorado. The role mixes onsite and remote work with 8-10 days on site per month and up to 60% travel. A 2-year monitoring track and related degree are required.

You will monitor sites, ensure protocol compliance, manage CRFs, and coordinate with vendors and study teams across multiple sites. The position emphasizes data quality and regulatory adherence in a fast-paced environment.