Clinical Research Associate II, Phase I - Texas/Mid-West
$100k - $120kFortrea
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
Vacancy posted 19 days ago
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