Centralized Clinical Team Lead I / Centralized Clinical Team Lead II - Ukraine
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.
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.