Site Supervisor - Orlando

Position Summary The Site Supervisor provides day‑to‑day leadership and operational oversight for site staff supporting the PMTA study. This role holds primary accountability for site‑level protocol execution, regulatory compliance, investigational product control, and staff performance. Key Responsabilities Provide direct supervision and day‑to‑day management of site staff supporting the PMTA study Work with Facility Director/Manager to assign, oversee, and balance staff responsibilities to ensure adequate coverage for subject visits and study activities Monitor staff performance and adherence to study protocols, SOPs, and regulatory requirements Maintain overall responsibility for site‑level compliance with the study protocol, applicable SOPs, and regulatory requirements Ensure informed consent is obtained and documented correctly for all subjects prior to any study‑related procedures Oversee the accuracy, completeness, and maintenance of all regulated study documentation and source records Oversee subject screening, enrollment, and retention activities to ensure consistent, compliant execution Work with Clinical Project Management team to support complex subject interactions, escalated concerns, or compliance‑related issues High school diploma required College degree preferred or equivalent relevant work experience Prior experience in clinical research, market research, or regulated study environments required Previous supervisory or lead experience strongly preferred #J-18808-Ljbffr 卡杯