FSP Clinical Research Associate 2 - Oncology

Fortrea seeks experienced Clinical Research Associates to monitor clinical trial sites near major US hub airports. This role involves 8-10 days on-site monthly, combining remote and in-person work, with responsibility for site management, data integrity, and regulatory compliance across multiple studies.

Responsibilities

• Monitor clinical sites including routine visits, initiation, close-out, and file maintenance
• Verify informed consent procedures and protocol adherence per regulatory requirements
• Review Case Report Forms for data integrity and generate queries against established guidelines
• Process and follow up on Serious Adverse Event reporting and documentation
• Ensure study staff receive proper training and materials for safe patient enrollment

Requirements

• University or college degree or certification in allied health profession (e.g., nursing licensure)
• 2 years of clinical monitoring experience
• Comfortable with 60% overnight travel to client sites
• Proficiency with electronic data collection systems and computer software
• Strong organizational skills to manage competing priorities in fast-paced environment
• Effective communication and teamwork abilities

Compensation: $100,000-$112,000