Sr Clinical Research Associate I, Phase I
$100k - $130kFortrea
Fortrea seeks a Senior Clinical Research Associate with 3+ years of clinical monitoring experience and Phase I trial background for their Durham, North Carolina office. The role involves site monitoring, data integrity oversight, protocol adherence verification, and adverse event reporting across multiple clinical research projects with frequent travel requirements.
Responsibilities
- Monitor clinical sites including routine monitoring, close-out, file maintenance, and initiation visits
- Verify informed consent procedures and protocol adherence per regulatory requirements
- Review Case Report Forms for data integrity and generate queries against established guidelines
- Complete Serious Adverse Event reporting, narratives, and follow-up documentation
- Coordinate clinical projects as Local Project Coordinator and assist with training new employees
Requirements
- University or college degree, or allied health certification (e.g. nursing licensure)
- 3+ years of clinical monitoring experience
- Phase I trial experience required
- Ability to travel 40-50% overnight domestically and internationally
- Proficiency with electronic data systems and computer software
- Valid driver's license and ability to operate vehicle safely
Compensation: $100,000–$130,000
Vacancy posted 11 days ago
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