Clinical Research Regulatory Specialist

Job is Expired
Location: Remote
Compensation: Hourly
Reviewed: Thu, Apr 24, 2025

Job Summary

A company is looking for a Clinical Research Regulatory Specialist.

Key Responsibilities
  • Prepares and maintains regulatory binders for audits and reviews
  • Maintains required regulatory documentation for studies and sponsors
  • Submits Adverse Event Reports and Protocol Deviations in compliance with requirements
Required Qualifications
  • Bachelor's degree
  • 3 years of relevant experience
  • Basic understanding of FDA and OHRP regulations and ICH guidelines
  • Experience with regulatory processing and submissions
  • Adept at learning new technologies

COMPLETE JOB DESCRIPTION

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