Clinical Research Associate II, Phase I - Texas/Mid-West
Fortrea · Topeka, KS
Clinical OperationsFull timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
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.
What they're looking for
- 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
What you'll be doing
- 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
Compensation$100,000-$120,000
Privacy & handoff
This role links to Fortrea's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.