Clinical Research Coordinator II

Tulane group

New Orleans (LA)

On-site

USD 60,000 - 76,000

Full time

8 hours ago
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Job summary

Tulane University is seeking a Clinical Research Coordinator II to manage all aspects of conducting clinical trials in New Orleans, LA. The role requires in-depth protocol knowledge and adherence to good clinical practices, acting as a liaison between patients, investigators, IRB and sponsor.

The position involves screening, enrolling and following study patients under supervision, with data and regulatory file maintenance, including adverse event reporting.

Qualifications

  • Bachelor's degree or RN with current Louisiana state licensure at the time of hire and one year of related work experience
  • OR LPN with current Louisiana state licensure at the time of hire and four years of related work experience
  • Preferred qualification: knowledge of IRB submission process and requirements
  • Knowledge of good clinical practices as set forth by federal regulations

Responsibilities

  • Manage all aspects of conducting clinical trials.
  • Screen, enroll and follow study patients under supervision to ensure protocol compliance and patient monitoring.
  • Maintain data and source documentation and regulatory files, including adverse event reporting, under direct supervision.
  • Liaise between patient, investigator, IRB and sponsor to support trial activities

Skills

Protocol requirements
Good clinical practices
IRB submission knowledge

Education

Bachelor's degree
RN with LA licensure
LPN with LA licensure

Job description

The primary responsibility of the Clinical Research Coordinator II is to manage all aspects of conducting clinical trials. The Clinical Research Coordinator II is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As one of the primary resources for the protocol, the Clinical Research Coordinator II acts as a liaison between the patient, investigator, Institutional Review Board and sponsor. The Clinical Research Coordinator II is able to screen, enroll and follow study patients, under supervision, ensuring protocol compliance and close patient monitoring, continuing the required learning process record in this second level position for advancement towards a Clinical Research Coordinator III position. The Clinical Research Coordinator is responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files, under direct supervision.

Responsibilities
Qualifications
  • Minimum Qualification:
  • Bachelor's degree or RN with current Louisiana state licensure at the time of hire and one (1) year of related work experience
  • OR
  • LPN with current Louisiana state licensure at the time of hire and four (4) years of related work experience
  • Preferred Qualification:
  • Knowledge of IRB submission process and requirements
  • Knowledge of good clinical practices as set forth by federal regulations
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 hr@tulane.edu .

Job Info
  • Job Identification 2064
  • Job Category Research
  • Posting Date 10/05/2026, 09:45 PM
  • Degree Level Bachelor's Degree
  • Job Schedule Full time
  • Job Shift Day
  • Locations New Orleans, LA, United States
  • Legal Employer Tulane University
  • Business Unit Tulane University
  • Department SOM LACaTS Clinical Research Resources Core
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