Clinical Research Associate II, Phase I

Fortrea seeks a Clinical Research Associate II with Phase I experience for on-site monitoring in Durham, North Carolina. The role involves managing clinical trial sites, ensuring protocol compliance, monitoring data integrity, and coordinating study activities with 40-50% overnight travel required.

Responsibilities Monitor clinical sites through routine visits, initiation meetings, and close-out procedures Verify informed consent procedures and protocol adherence per regulatory standards Review Case Report Forms for data accuracy and generate queries for discrepancies Process Serious Adverse Event reporting, narratives, and follow-up documentation Coordinate with study staff, vendors, and sites to ensure proper trial execution Requirements University degree or allied health certification (e.g., nursing licensure) 1+ years of clinical monitoring experience Phase I trial experience Ability to travel 40-50% overnight, including domestic and international Proficiency with electronic data management systems Valid driver's license and safe driving ability Compensation:

$105,000-$118,000