We are looking for an experienced Centralized Clinical Team Lead I / Centralized Clinical Team Lead II, to oversee and drive performance within our Central Monitoring team, ensuring high-quality data review and efficient study oversight. Main Responsibilities Lead, mentor, and develop a team of Central Monitors, ensuring high performance and engagement Oversee centralized monitoring activities, including data review, risk identification, and issue escalation Ensure delivery of monitoring outputs in line with study timelines, quality standards, and regulatory requirements Collaborate cross-functionally (e.g., Clinical Operations, Data Management, Biostatistics) to support study execution Drive risk-based monitoring strategies and continuous process improvements Support resource planning, workload allocation, and capacity management across studies Contribute to quality oversight by identifying trends, implementing corrective actions, and supporting audits/inspections Experience Required Bachelor’s degree in Life Sciences or related field Proven experience in centralized monitoring or clinical data review within a CRO or pharma environment Previous people management or team leadership experience Strong knowledge of ICH-GCP guidelines and risk-based monitoring approaches Excellent stakeholder management, communication, and problem-solving skills Learn more about our EEO & Accommodations request here.