Oversee day-to-day operations at multiple clinical research sites within the region.
Ensure trials are conducted in full compliance with Good Clinical Practice (GCP), FDA, ICH, and protocol requirements.
Lead all phases of clinical trial execution including site initiation, monitoring, subject recruitment, and study close-out.
Ensure consistent, high-quality data collection and timely patient enrollment across all sites.
Lead, mentor, and support site-level teams, including Principal Investigators, Clinical Research Coordinators, and other staff.
Promote a collaborative and high-performance work culture through coaching, development, and team-building.
Proactively resolve site-level challenges and performance issues.
Ensure strict adherence to study protocols, IRB/ethics board guidelines, and applicable federal regulations.
Conduct internal site audits and oversee corrective actions when necessary.
Maintain accurate and timely documentation, including ICFs, AEs, SAEs, and source documents.
Manage site budgets and ensure adherence to financial agreements.
Support contract negotiations and oversee invoicing and payment processes.
Collaborate with sponsors, CROs, and internal departments to ensure seamless clinical trial execution.
Monitor site performance metrics (e.g., enrollment, retention, data quality) and provide regular reports to leadership.

Minimum 5 years of clinical research experience, with 1+ years in a leadership role required
Multi-site management experience preferred
Demonstrated expertise in overseeing multiple clinical research trials across varying therapeutic areas required
Strong understanding of GCP, FDA regulations, ICH guidelines, and industry best practices required
Bachelor’s Degree preferred, or equivalent combination of education, training and experience.

Region Manager

Key skills