Clinical Research Associate II, Phase I

Fortrea

Clinical Research Associate managing site monitoring for clinical trials in Phase I studies. Ensuring compliance with regulatory standards and providing high-quality care for study participants.

Posted 6/3/2026full-timeRemote • Kansas, Texas • 🇺🇸 United StatesJuniorMid-Level💰 $105,000 - $118,000 per yearWebsite

About the role

Key responsibilities & impact

Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites
Conduct pre-study and initiation visits
Ensure informed consent procedures and protocol requirements are adhered to
Monitor data for missing or implausible data
Complete Serious Adverse Event (SAE) reporting
Assist with training of new employees

Requirements

What you’ll need

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
1+ years of Clinical Monitoring experience
Phase I experience
40-50% overnight travel

Benefits

Comp & perks

Health insurance
Flexible work arrangements
Professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical monitoringdata monitoringSAE reportinginformed consent proceduresprotocol adherencepre-study visitsinitiation visits

Soft Skills

trainingcommunication

Certifications

nursing licensure