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Clinical Research Regulatory Coordinator

ochsner · New Orleans - New Orleans Region - Louisiana

New
Onsite Mid 🇬🇧 English
Epic

Job description

About the role

The Clinical Research Regulatory Coordinator independently manages and coordinates all aspects of clinical trials for selected departments, ensuring compliance with federal, state, and institutional regulations.

Key responsibilities

  • Manage research activities associated with clinical trials, including data management and study start‑up.
  • Maintain study compliance, oversee regulatory processes, and participate in internal and external audits.
  • Coordinate grant and budget development, and track special projects.
  • Maintain strong relationships with study sponsors and seek continuing education opportunities.

Required profile

  • High school diploma or equivalent.
  • 3 years of relevant clinical research experience, or 2 years with ACRP/SOCRA certification.
  • Strong critical‑thinking, organizational, and communication skills.
  • Ability to travel between facilities and work flexible schedules.

Required skills

  • Proficiency with Epic electronic health record system.
  • Experience using computers, software, and web‑based applications for research management.

Questions fréquentes

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Source : ats:workday

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Published 7 hours ago

Expires 1 month from now

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ochsner

New Orleans - New Orleans Region - Louisiana

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