Clinical Research Associate II, Phase I - Texas/Mid-West

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