Site Supervisor - Atlanta

Sago • Atlanta, GA

3h • Onsite

About The Position

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.

Requirements

• High school diploma required
• Prior experience in clinical research, market research, or regulated study environments required

Nice To Haves

• College degree preferred or equivalent relevant work experience
• Previous supervisory or lead experience strongly preferred

Responsibilities

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED