Regulatory Coordinator

Employer
Tulane University
Location
New Orleans, LA

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Employment Type
Full Time
Institution Type
Four-Year Institution
Regulatory CoordinatorLACATS Clinical Research Resources Core

Location: New Orleans, LA

Summary

The Regulatory Coordinator is a full-time staff member who participates in the development, implementation and regulatory compliance maintenance of clinical research trials for multiple sites and studies of different therapeutic areas and phases in accordance with appropriate regulations, Standard Operating Procedures (SOP'S), and study specific protocols/plans and processes. The Regulatory Coordinator will be required to complete Good Clinical Practices (GCP) training, and additional specialized regulatory training, sponsor training on protocol requirements, etc.

Required Qualifications

Bachelor's degree or RN with current Louisiana state licensure at the time of hire and three (3) years of related work experience, including two (2) years of direct regulatory experience OR LPN with current Louisiana state licensure at the time of hire and six (6) years of related work experience; or a Master™s degree and two (2) years of related work experience

Preferred Qualifications

Certification as a Certified Clinical Research Coordinator (CCRC through the Association of Clinical Research Professionals or ACRP) OR Certified Clinical Research Professional (CCRP through the Society of Clinical Research Associates or SoCRA) is preferredRegulatory Affairs Certification (RAC), Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or Certified IRB Professional (CIP) preferred

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