Clinical Research Associate II, Phase I Job at Fortrea, Durham, NC

  • Fortrea
  • Durham, NC

Job Description

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

Job Tags

Night shift

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