Clinical Research Coordinator, MH-CIP (Spanish-speaking preferred)
Company: Tulane University
Location: New Orleans
Posted on: April 25, 2025
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Job Description:
Clinical Research Coordinator, MH-CIP (Spanish-speaking
preferred)Epidemiology Location: New Orleans, LA 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. Required Qualifications The education required
for each level is listed below:
Clinical Research Coordinator I (Pay Grade 23)*Licensed Practical
Nurse with current state licensure at the time of hire and 3 years
of related work experienceOR*Bachelor's Degree or Registered Nurse
with current state licensure at the time of hire
Clinical Research Coordinator II (Pay Grade 24)*Licensed Practical
Nurse with current state licensure at the time of hire and 4 years
of related work experienceOR*Bachelor's Degree or Registered Nurse
with current state licensure at the time of hire and 1 year of
related work experienceOR*Master's Degree in a related field
Clinical Research Coordinator III (Pay Grade 25)*Licensed Practical
Nurse with current state licensure at the time of hire and 5 years
of related work experienceOR*Bachelor's Degree or Registered Nurse
with current state licensure at the time of hire and 2 years of
related work experienceOR*Master's Degree in a related field and 1
year of related experience Preferred Qualifications
FOR ALL LEVELS: Spanish language fluency-oral and writtenLevel
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 PandoLogic. Keywords: Clinical
Research Coordinator, Location: New Orleans, LA - 70116 , PL:
597492622
Keywords: Tulane University, Kenner , Clinical Research Coordinator, MH-CIP (Spanish-speaking preferred), Healthcare , New Orleans, Louisiana
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