Onsite Study Supervisor (Temporary)

Sago

Baltimore (MD)

On-site

USD 28,000 - 40,000

Full time

3 days ago
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Job summary

Sago is seeking a Site Supervisor to lead day-to-day operations for the PMTA study at an on-site Maryland location. This temporary, full-time role focuses on protocol execution, regulatory compliance, investigational product control, and staff performance, with on-site supervision as a core duty.

The position starts August 1, 2026 and ends February 28, 2027, with a pay rate of $25 per hour. Strong leadership, regulatory knowledge, and attention to detail are essential for success.

Qualifications

  • 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.
  • Strong computer literacy, including proficiency with Microsoft Office and study-related systems.
  • Leadership & Accountability
  • Regulatory Knowledge
  • Communication
  • Organization & Planning
  • Attention to Detail

Responsibilities

  • Supervise site staff and daily study activities.
  • Balance staffing to ensure coverage for subject visits and activities.
  • Monitor staff performance and adherence to protocols and regulatory requirements.
  • Escalate operational issues and protocol clarifications as primary contact.
  • Maintain site-level compliance with study protocol and SOPs.
  • Ensure informed consent is obtained and documented for all subjects.
  • Maintain accurate study documentation and source records.
  • Prepare for monitoring visits and audits.

Skills

Leadership
Regulatory Knowledge
Communication
Organization & Planning
Attention to Detail

Education

High school diploma
College degree preferred or equivalent

Tools

Microsoft Office

Job description

Sago is seeking a Site Supervisor to lead day-to-day operations for the PMTA study at an on-site Maryland location. This temporary, full-time role focuses on protocol execution, regulatory compliance, investigational product control, and staff performance, with on-site supervision as a core duty.

The position starts August 1, 2026 and ends February 28, 2027, with a pay rate of $25 per hour. Strong leadership, regulatory knowledge, and attention to detail are essential for success.

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