Temporary On-Site Study Supervisor (Clinical Research)

Sago; Baltimore (MD); Hybrid; USD 29,000 - 39,000; Full time

Job summary

Sago, formerly Schlesinger Group, is seeking a Site Supervisor to lead day-to-day operations for the PMTA study at our Baltimore area site. This on-site leadership role oversees protocol execution, regulatory compliance, IP control, and staff performance.

The temporary full-time position pays $25 per hour, with start date August 01st, 2026 and end date February 28th, 2027. The role ensures staff coverage, adherence to SOPs, and preparation for monitoring visits and audits.

Qualifications

• High school diploma required.
• College degree preferred or equivalent relevant work experience.
• Experience in clinical research, market research, or regulated study environments required.
• Previous supervisory or lead experience preferred.
• Strong computer literacy with Microsoft Office and study-related systems.

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.
• Prepare for, support, and participate in monitoring visits and audits.
• 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 escalation 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.

Skills

Leadership

Communication

Attention to Detail

Organization & Planning

Regulatory Knowledge

Education

High school diploma required

College degree preferred

Tools

Microsoft Office

Study-related systems

Job description

Sago, formerly Schlesinger Group, is seeking a Site Supervisor to lead day-to-day operations for the PMTA study at our Baltimore area site. This on-site leadership role oversees protocol execution, regulatory compliance, IP control, and staff performance.

The temporary full-time position pays $25 per hour, with start date August 01st, 2026 and end date February 28th, 2027. The role ensures staff coverage, adherence to SOPs, and preparation for monitoring visits and audits.