Clinical Research Coordinator III

Tulane University Translational Science Institute; New Orleans (LA); On-site; USD 70,000 - 90,000; Full time

Job summary

Tulane University Translational Science Institute is seeking a Clinical Research Coordinator III to manage all aspects of clinical trials with minimal supervision in a fast-paced environment.

You will serve as the protocol's primary resource, liaising among patients, investigators, IRB and sponsor, ensuring protocol compliance and thorough monitoring throughout study conduct.

Qualifications

• Bachelor’s degree or RN with Louisiana state licensure at hire and two years of related work experience.
• Or LPN with Louisiana state licensure at hire and five years of related work experience.
• Or Master’s degree and one year of related work experience.
• Certification as CCRC (ACRP) or CCRP (SoCRA) strongly desired.
• Supervisory experience preferred.

Responsibilities

• Responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files.
• Screens, enrolls and follows study patients, ensuring protocol compliance and close patient monitoring.
• Acts as liaison between patient, investigator, IRB and sponsor for protocol adherence.
• Designs, coordinates and implements assigned research projects with minimal supervision.
• Maintains knowledge of protocol requirements and Good Clinical Practice per federal regulations.

Skills

GCP knowledge

IRB submission process

Patient interaction

CITI training

Institutional credentialing

Education

Bachelor’s degree or RN with LA licensure + 2 years related experience

LPN with LA licensure + 5 years related experience

Master’s degree + 1 year related experience

Job description

The primary responsibility of the Clinical Research Coordinator III is to manage all aspects of conducting clinical trials, with minimal supervision. The Clinical Research Coordinator III is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for the protocol, the Clinical Research Coordinator III acts as a liaison between the patient, investigator, Institutional Review Board and sponsor. The Clinical Research Coordinator III screens, enrolls and follows study patients, ensuring protocol compliance and close patient monitoring, and works independently in designing, coordinating, and implementing all assigned research projects. The Clinical Research Coordinator III is responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files.

Responsibilities

• Knowledge of good clinical research practice is required
• In-depth knowledge of IRB submission process and requirements
• Must be able to interact well with patients and the general public
• Ability to acquire and maintain all required CITI training certificates
• Ability to acquire and maintain credentialing at all required institutions: Tulane Medical Center, Veterans Administration Hospital/New Orleans, LA and University Medical Center

Qualifications

Minimum Qualification:

• Bachelor’s degree or RN with current Louisiana state licensure at the time of hire and two (2) years of related work experience.
• Or
• LPN with current Louisiana state licensure at the time of hire and five (5) years of related work experience.
• Or
• Master’s degree and one (1) year of related work experience

Preferred Qualification:

• 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 strongly desired
• Supervisory experience is preferred

About Us

Tulane University is an equal opportunity educator and employer committed to providing an education and employment environment free of unlawful discrimination, harassment, and retaliation. Legally protected demographic classifications (such as a person’s race, color, religion, age, sex, national origin, shared ancestry, disability, genetics, veteran status, or any other characteristic protected by federal, state, or local laws) are not relied upon as an eligibility, selection or participation criteria for Tulane’s employment or educational programs or activities.

Tulane University is responsible for providing reasonable accommodations to individuals with disabilities throughout the applicant screening process. If you need assistance in completing an application or during any phase of the interview process, please contact the Office of Human Resources by phone at 504-865-4748 or by email at [e-mail].

Job Info

• Job Identification 1355
• Job Category Research
• Posting Date 07/22/2026, 07:23 PM
• Job Schedule Full time
• Job Shift Day
• Locations New Orleans, LA, United States
• Legal Employer Tulane University
• Business Unit Tulane University
• Department SOM Medicine - Tulane Research Innovation for Arrhythmia Discoveries (TRIAD)