Temporary Office and Site Supervisor - Baltimore

Start date: August 01st, 2026

End date: February 28th, 2027

Key Responsibilities: Provide direct supervision and day-to-day management of site staff supporting the PMTA study 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 Serve as the primary escalation point for staff questions, operational issues, and protocol clarifications 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 Identify, document, and escalate protocol deviations, compliance risks, and required corrective actions in accordance with study and regulatory standards 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 Ensure subject visits are conducted within protocol-defined windows and procedural requirements Oversee subject visit scheduling, staffing plans, and workflow to meet study timelines and enrollment goals Ensure site readiness for scheduled visits, including materials, staffing, documentation, and IP availability Act as the primary site-level point of contact for Clinical Project Managers and study monitors Prepare for, support, and participate in monitoring visits and audits Respond to monitor queries, action items, and follow-up requests within established timelines