FSP Sr. Clinical Research Associate II - West Coast - Ophthalmology
$125k - $140kFortrea
Fortrea seeks a senior clinical research associate with 5+ years of monitoring experience to oversee oncology clinical trial sites across Colorado, Nevada, and Utah. The role involves comprehensive site management, protocol compliance verification, data integrity oversight, and serious adverse event reporting.
Responsibilities
- Monitor and manage clinical trial sites including routine visits, close-out, and file maintenance
- Verify informed consent procedures and protocol adherence at sites
- Review case report forms for data integrity and generate resolution queries
- Complete serious adverse event reporting and follow-up documentation
- Coordinate designated clinical projects and serve as local client contact as assigned
Requirements
- University or college degree or certification in allied health profession
- 5+ years of clinical monitoring experience
- Oncology experience, early phase preferred
- Ability to travel 30-50% overnight
- Proficiency with electronic data collection systems
- Strong communication and teamwork skills
Compensation: $125,000-$140,000
$125k - $140k
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