Clinical Research Associate II, Phase I
$105k - $118kFortrea
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
Vacancy posted 5 days ago
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