Clinical Research Associate II, Phase I — Fast-Paced Trials

Fortrea; Topeka (KS); On-site; USD 100,000 - 120,000; Full time

Job summary

Fortrea seeks a Clinical Research Associate with 1+ years of clinical monitoring experience. Phase I experience is preferred, with 40–50% overnight travel. You will monitor sites, ensure regulatory compliance, and support data integrity across trials.

Qualifications include a university degree or allied health certification. The role involves coordinating with teams and vendors in a fast-paced clinical research environment.

Qualifications

• 1+ years of Clinical Monitoring experience.
• Phase I experience preferred.
• University degree or related allied health certification.
• Willingness to travel 40–50% overnight.

Responsibilities

• Monitor study sites, conduct pre-study and initiation visits, and maintain study files.
• Oversee site management per project plans and liaise with vendors.
• Perform general on-site monitoring and ensure staff adherence to protocol.
• Verify informed consent procedures and regulatory compliance.
• Review CRFs and monitor data for accuracy.
• Manage registries and assist with feasibility activities.
• Complete SAE reporting and follow-up as required.
• CRF review, queries, and data quality checks per guidelines.
• Assist with training and coordinate local project activities.

Skills

Clinical Monitoring

Phase I Experience

Education

University degree or allied health certification

Job description

Fortrea seeks a Clinical Research Associate with 1+ years of clinical monitoring experience. Phase I experience is preferred, with 40–50% overnight travel. You will monitor sites, ensure regulatory compliance, and support data integrity across trials.

Qualifications include a university degree or allied health certification. The role involves coordinating with teams and vendors in a fast-paced clinical research environment.