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 ResponsibilitiesLead 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 analysisAct as quality events owners driving on-time closureAct 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 GCPQualificationsUniversity/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.