Senior CRA II - Ophthalmology/Oncology (Travel-Heavy)

Fortrea; Oregon; Hybrid; USD 125,000 - 142,000; Full time

Job summary

Fortrea is seeking a Senior Clinical Research Associate (CRA) with 4+ years of site monitoring experience. The role includes on-site and remote activities across multiple US regions, with substantial overnight travel to Denver, CO, Chicago, IL, Des Moines, IA, or Kansas City, MO.

You will ensure protocol compliance and data integrity within a fast-paced clinical trials environment. The position emphasizes monitoring quality, safety oversight, and collaboration with cross-functional teams.

Qualifications

• Must have 4+ years of Clinical Monitoring experience.
• Willingness to travel 30-50% overnight.
• Strong teamwork and communication skills.

Responsibilities

• Oversee all aspects of site monitoring, visits, and data quality.
• Manage site coordination and liaison with vendors as required.
• Ensure informed consent and protocol adherence according to regulatory standards.
• Review CRFs and data for accuracy; address data queries.
• Provide training support and act as local contact on assigned projects.

Skills

Clinical Monitoring

Overnight travel willingness

Team collaboration

Education

Bachelor’s degree or allied health certification

Tools

EDC systems

Job description

Fortrea is seeking a Senior Clinical Research Associate (CRA) with 4+ years of site monitoring experience. The role includes on-site and remote activities across multiple US regions, with substantial overnight travel to Denver, CO, Chicago, IL, Des Moines, IA, or Kansas City, MO.

You will ensure protocol compliance and data integrity within a fast-paced clinical trials environment. The position emphasizes monitoring quality, safety oversight, and collaboration with cross-functional teams.