Clinical Research Coordinator (I, II, and III) Position Available In Orleans, Louisiana
Tallo's Job Summary: The Clinical Research Coordinator (I, II, and III) in Epidemiology based in New Orleans, LA, coordinates and conducts clinical studies in cardiovascular and chronic kidney diseases. Responsibilities include developing study protocols, enrolling participants, data collection, and maintaining regulatory files. Required qualifications vary by level, with Pay Grades 23-25. Preferred qualifications include Spanish language fluency and certification as a Certified Clinical Research Coordinator for higher levels.
Job Description
Clinical Research Coordinator (I, II, and III)
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 in cardiovascular and chronic kidney diseases. 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 documentations, 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)
- 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 (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 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 (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 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
- 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
