FSP Sr. Clinical Research Associate II - Midwest - Ophthalmology & Oncology
$125k - $140kFortrea
Fortrea seeks a senior clinical research associate with 5+ years of monitoring experience for ophthalmology and oncology trials in the Midwest. This role involves comprehensive site monitoring, protocol compliance verification, data integrity oversight, and serious adverse event reporting across multiple clinical trial sites.
Responsibilities
- Conduct routine monitoring and close-out activities at clinical trial sites
- Verify informed consent procedures and protocol adherence by study staff
- Review Case Report Forms for data accuracy and completeness
- Complete Serious Adverse Event reporting and follow-up documentation
- Coordinate with study sites and vendors on project implementation
Requirements
- University degree or allied health certification (e.g., nursing licensure)
- 5+ years of clinical monitoring experience
- Oncology experience with early phase preference
- Ability to travel 30-50% overnight
- Proficiency with electronic data capture systems and computer software
- Strong organizational and teamwork skills
Compensation: $125,000-$140,000
Vacancy posted 13 days ago
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