What are the responsibilities and job description for the Clinical Research Coordinator I, II & III (CHERISH) position at Tulane University Staff?
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, performs noninvasive cardiovascular tests according to study protocols, and conducts small group coaching sessions. 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
Willing to travel to conduct church visits
o This role involves travel most days to churches in the greater New Orleans area
o Staff are reimbursed for travel
The education required for each level is listed below :
Clinical Research Coordinator I (Pay Grade 23)
Bachelor's Degree or RN with current state licensure at the time of hire
LPN with current state licensure at the time of hire and three (3) years of related work experience
Clinical Research Coordinator II (Pay Grade 24)
Bachelor's Degree or RN with current state licensure at the time of hire and one (1) year of related work experience
LPN with current state licensure at the time of hire and four (4) years of related work experience
Master's Degree in a related field
Clinical Research Coordinator III (Pay Grade 25)
Bachelor's Degree or RN with current state licensure at the time of hire and two (2) years of related work experience
LPN with current state licensure at the time of hire and five (5) years of related work experience
Master's Degree and one (1) year of related work experience
Level I
Expressed interest in Clinical Research
Motivated to learn about Clinical Research and associated regulations
Preferred Spanish language fluency-oral and written
Level II
Knowledge of IRB submission process and requirements
Knowledge of good clinical practices as set forth by federal regulations
Preferred Spanish language fluency-oral and written
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
Preferred Spanish language fluency-oral and written
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