Job Listings

Clinical Research Coordinator

Company:
Tulane University
Job Location:
New Orleans, Louisiana
Category:
Laboratory and Research
Epidemiology
Location: Hammond, LA

Summary

The primary responsibility of the Clinical Research Coordinator is to manage all aspects of conducting clinical trials. The Clinical Research Coordinator 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 acts as a liaison between the patient, investigator, Institutional Review Board and sponsor. The Clinical Research Coordinator 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 is responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files.

Required Knowledge, Skills, and Abilities:
  • Knowledge of good clinical research practice
  • 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
Required Education and/or Experience:

The education required for each level is listed below:

Clinical Research Coordinator I

  • Bachelor's degree or RN with current state licensure at the time of hire

OR

  • LPN with current state licensure at the time of hire and three (3) years of related work experience

Clinical Research Coordinator II

  • Bachelor's degree or RN with current state licensure at the time of hire and one (1) year of related work experience

OR

  • LPN with current state licensure at the time of hire and four (4) years of related work experience

OR

  • Master's degree in a related field

Clinical Research Coordinator III

  • Bachelor's degree or RN with current state licensure at the time of hire and two (2) years of related work experience

OR

  • LPN with current 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 Qualifications:

Level I

  • Expressed interest in Clinical Research
  • Motivated to learn about Clinical Research and associated regulations

Level II

  • Knowledge of IRB submission process and requirements
  • Knowledge of good clinical practices as set forth by federal regulations

Level III

  • 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)
  • Supervisory experience
Compensation Information
This position is assigned to pay grade T4.25. Tulane offers a variety of options to enhance your health and well-being so that
you may enjoy more out of life now and in the future. Learn more about Life at Tulane
as well as our Benefits and Pay. See our
Candidate Resources to learn more about our hiring process and what to expect.

How to Apply:
Click "Apply Now" to apply for this job.

This position will close onthe date it is filled

Tulane University is an EOE/M/F/Vet/Disabled employer with a strong commitment to diversity and inclusion. Applications by members of all underrepresented groups are encouraged.
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