More jobs:
Clinical Research Coordinator, MH-CIP; Spanish-speaking
Job in
New Orleans, Jefferson Parish, Louisiana, 70123, USA
Listed on 2026-02-16
Listing for:
Tulane University
Full Time
position Listed on 2026-02-16
Job specializations:
-
Healthcare
Clinical Research -
Research/Development
Clinical Research
Job Description & How to Apply Below
Location: New Orleans
Summary
The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials related to maternal health and diabetes. The Clinical Research Coordinator assists the investigator team to develop study protocols and manuals of procedures. The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and entry, and performs noninvasive cardiovascular tests according to study protocols.
The Clinical Research Coordinator is also responsible for keeping all data and source documentation, adverse event reporting, and IRB regulatory files.
- 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
- Licensed Practical Nurse with current state licensure at the time of hire and 3 years of related work experience
- OR
- Bachelor’s Degree or Registered Nurse with current state licensure at the time of hire
- Licensed Practical Nurse with current state licensure at the time of hire and 4 years of related work experience
- OR
- Bachelor’s Degree or Registered Nurse with current state licensure at the time of hire and 1 year of related work experience
- OR
- Master’s Degree in a related field
- Licensed Practical Nurse with current state licensure at the time of hire and 5 years of related work experience
- OR
- Bachelor’s Degree or Registered Nurse with current state licensure at the time of hire and 2 years of related work experience
- OR
- Master’s Degree in a related field and 1 year of related experience
Spanish language fluency-oral and written Level I
- Expressed interest in Clinical Research
- Motivated to learn about Clinical Research and associated regulations
- Knowledge of IRB submission process and requirements
- Knowledge of good clinical practices as set forth by federal regulations
- 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
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