"Regulatory Coordinator, Clinical Trials Office - Tulane Cancer Center"

Job Details

Regulatory Coordinator, Clinical Trials Office - Tulane Cancer Center

Tulane Cancer Center - Clinical Trials Office (CTO)

Location: New Orleans, LA

Summary

Under the direction of the Executive Director of the Clinical Trials Office (CTO) or their designee, the Regulatory Coordinator independently performs administrative and coordinative work directed toward the design, implementation, evaluation, and review of assigned Tulane Cancer Center (TCC) clinical trials by working closely with Principal Investigators (PI) and other CTO staff members. The Regulatory Specialist provides operational support for regulatory compliance and is able to independently provide regulatory support to the TCC PI and research sites conducting multiple FDA-regulated or other clinical trials. This position is able to successfully manage a workload that includes all trial types and mentor other Regulatory Coordinators. This classification requires the use of judgment and discretion in performing the assigned duties and responsibilities related to the projects. The Regulatory Coordinator works with the PI and CTO staff with moderate to minimal supervision and direction.

Required Qualifications

Bachelor’s degree and three (3) years of clinical research related experience; or RN with current Louisiana state licensure at the time of hire and three (3) years of clinical research related experience; or LPN with current Louisiana state licensure at the time of hire and six (6) years of clinical research related experience; or a Master’s degree and two (2) years of clinical research related experience

Preferred Qualifications

• Master’s degree in Public Health, Business or Social work preferred.
• Two or more years of oncology clinical research coordination/related experience
• Clinical Research Certification (e.g., SOCRA, ACRP, etc.)