Regulatory Coordinator
- Employer
- Tulane University
- Location
- New Orleans, LA
View more
- Employment Type
- Full Time
- Institution Type
- Four-Year Institution
Location: New Orleans, LA
SummaryThe 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 QualificationsBachelor'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 experienceORLPN with current Louisiana state licensure at the time of hire and six (6) years of related work experience; or a MasterÃÂs degree and two (2) years of related work experience
Preferred QualificationsCertification 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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