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
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Regulatory Coordinator, Clinical Trials Office - Tulane Cancer Center
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Tulane University .
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 involves working closely with Principal Investigators (PI) and other CTO staff members. 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 and responsibilities related to the projects. The Regulatory Coordinator works with the PI and CTO staff with moderate to minimal supervision and direction.
Required Knowledge, Skills, and Abilities
Excellent written and verbal communication skills.
Excellent computer literacy skills, including knowledge of standard office software.
Knowledge of IRB submission process and requirements.
Required Education and/or Experience
Bachelor’s degree and three (3) years of clinical research related experience; or
RN with current Louisiana state licensure and three (3) years of clinical research related experience; or
LPN with current Louisiana state licensure and six (6) years of clinical research related experience; or
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.).
Additional Details
Seniority level: Entry level
Employment type: Full-time
Job function: Legal
Industries: Higher Education
This job posting is active. Referrals can increase your chances of interviewing at Tulane University.
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Regulatory Coordinator, Clinical Trials Office - Tulane Cancer Center
role at
Tulane University .
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 involves working closely with Principal Investigators (PI) and other CTO staff members. 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 and responsibilities related to the projects. The Regulatory Coordinator works with the PI and CTO staff with moderate to minimal supervision and direction.
Required Knowledge, Skills, and Abilities
Excellent written and verbal communication skills.
Excellent computer literacy skills, including knowledge of standard office software.
Knowledge of IRB submission process and requirements.
Required Education and/or Experience
Bachelor’s degree and three (3) years of clinical research related experience; or
RN with current Louisiana state licensure and three (3) years of clinical research related experience; or
LPN with current Louisiana state licensure and six (6) years of clinical research related experience; or
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.).
Additional Details
Seniority level: Entry level
Employment type: Full-time
Job function: Legal
Industries: Higher Education
This job posting is active. Referrals can increase your chances of interviewing at Tulane University.
#J-18808-Ljbffr