Tulane University
Regulatory Coordinator, Clinical Trials Office - Tulane Cancer Center
Tulane University, New Orleans, Louisiana, United States, 70123
Regulatory Coordinator, Clinical Trials Office - Tulane Cancer Center
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 related to the design, implementation, evaluation, and review of Tulane Cancer Center (TCC) clinical trials. This role involves working closely with Principal Investigators (PI) and CTO staff. The Regulatory Specialist provides operational support for regulatory compliance and can independently support TCC PIs and research sites conducting FDA-regulated or other clinical trials. The position manages a workload that includes all trial types and mentors other Regulatory Coordinators. It requires judgment and discretion in performing duties related to 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 experience; or RN with current Louisiana state licensure and three (3) years of clinical research experience; or LPN with current Louisiana state licensure and six (6) years of clinical research experience; or Master’s degree and two (2) years of clinical research experience Preferred Qualifications
Master’s degree in Public Health, Business, or Social Work (preferred) Two or more years of oncology clinical research coordination or related experience Clinical Research Certification (e.g., SOCRA, ACRP, etc.)
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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 related to the design, implementation, evaluation, and review of Tulane Cancer Center (TCC) clinical trials. This role involves working closely with Principal Investigators (PI) and CTO staff. The Regulatory Specialist provides operational support for regulatory compliance and can independently support TCC PIs and research sites conducting FDA-regulated or other clinical trials. The position manages a workload that includes all trial types and mentors other Regulatory Coordinators. It requires judgment and discretion in performing duties related to 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 experience; or RN with current Louisiana state licensure and three (3) years of clinical research experience; or LPN with current Louisiana state licensure and six (6) years of clinical research experience; or Master’s degree and two (2) years of clinical research experience Preferred Qualifications
Master’s degree in Public Health, Business, or Social Work (preferred) Two or more years of oncology clinical research coordination or related experience Clinical Research Certification (e.g., SOCRA, ACRP, etc.)
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