Full-Time

Regulatory Coordinator

Georgetown University Medical Center

Posted on 12/13/2025

Deadline 3/19/26
Georgetown University

Georgetown University

Compensation Overview

$21.16 - $35.29/hr

Washington, DC, USA

In Person

On-Campus work designation; no remote option.

Category
Legal & Compliance (1)
Requirements
  • Bachelor’s degree in health science, life science, or related field
  • Minimum of 2 years of experience in regulatory affairs or clinical research
  • Familiarity with regulatory and ethical requirements related to human subjects research (e.g., IRB, FDA, ICH-GCP, IND/IDE)
  • Strong attention to detail and organizational skills
  • Excellent written and verbal communication.
  • Ability to manage multiple priorities and meet deadlines
  • Critical thinking and problem-solving abilities.
  • Proficiency in Microsoft Office and familiarity with regulatory databases
Responsibilities
  • Prepare and submit required regulatory documents (e.g., IRB applications, amendments, safety reports, protocol deviations)
  • Maintain accurate and up-to-date regulatory files for clinical research studies
  • Ensure compliance with institutional, federal, and sponsor regulations
  • Communicate with investigators, study staff, and regulatory agencies to support study approvals and updates
Desired Qualifications
  • Master’s degree or regulatory certification (e.g., SOCRA, ACRP)
  • Experience working in an academic medical center or large research institution
  • Knowledge of electronic regulatory systems and clinical trial management systems (e.g., OnCore, REDCap)
Georgetown University

Georgetown University

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