Clinical Research Associate II, Phase I - Texas/Mid-West Job at Fortrea, Topeka, KS

  • Fortrea
  • Topeka, KS

Job Description

Fortrea seeks a Clinical Research Associate II with Phase I experience to monitor clinical trial sites across Texas and the Mid-West. The role involves site management, protocol compliance verification, data integrity oversight, and serious adverse event reporting with 40-50% travel required.

Responsibilities

  • Monitor clinical sites including routine site visits, file maintenance, and protocol initiation
  • Verify informed consent procedures and protocol adherence at study sites
  • Review case report forms for data integrity and generate queries against data management systems
  • Complete and coordinate serious adverse event reporting and follow-up
  • Act as local project coordinator and client contact as assigned

Requirements

  • University or college degree or certification in allied health profession
  • 1+ years of clinical monitoring experience
  • Phase I trial experience
  • Willingness to travel 40-50% overnight
  • Proficiency with electronic data collection systems
  • Ability to work in fast-paced, changing priority environment

Compensation: $100,000-$120,000

Job Tags

Local area, Night shift

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