What are the responsibilities and job description for the Clinical Research Coordinator, MH-CIP (Spanish-speaking preferred) 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, 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
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 experience
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 experience
Bachelor's Degree or Registered Nurse with current state licensure at the time of hire and 1 year of related work experience
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 experience
Bachelor's Degree or Registered Nurse with current state licensure at the time of hire and 2 years of related work experience
Master's Degree in a related field and 1 year of related experience
FOR ALL LEVELS : Spanish language fluency-oral and written
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)
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