Centralized CTL

Fortrea is seeking a proactive and detail-oriented Centralized Clinical Team Lead I to join our Global Clinical Operations team. In this global role, you will lead central monitoring and other clinical operation activities across multiple clinical studies, ensuring high-quality execution and compliance with industry standards. You'll collaborate with cross-functional teams, drive process improvements, and play a key part in risk management and study analytics.

Key Responsibilities

• Lead and oversee central monitoring activities for multiple studies, ensuring accurate tracking and status reporting.
• Review monitoring visit reports, identify risks, and communicate trends or safety concerns to study teams.
• Manage protocol deviation review and trend analysis
• Act as quality events owners driving on-time closure
• Act as a liaison between CRAs, CTLs, and Project Managers for timely issue resolution.
• Support the creation of trip report templates, guidelines, and study documentation.
• Ensure compliance with Fortrea SOPs, ICH Guidelines, and GCP

• University/College Degree (Life Science preferred) or certification in an allied health profession.
• 2+ years of experience in trip report review and/or centralized/risk-based monitoring.
• 6-8 years of clinical research experience.
• Strong working knowledge of ICH GCP and regulatory requirements.
• Advanced computer skills (MS Office Suite).
• Excellent planning, organizational, and communication skills.
• Strong interpersonal and leadership abilities.

Learn more about our EEO & Accommodations request here.