Clinical Research Coordinator I, II & III (Covington, LA) Position Available In Orleans, Louisiana
Tallo's Job Summary: The Clinical Research Coordinator I, II & III positions in Covington, LA involve coordinating and conducting clinical studies related to maternal health and diabetes. Responsibilities include developing study protocols, enrolling participants, data collection, and regulatory compliance. Required qualifications vary by level, with pay grades ranging from 23 to 25. Preferred qualifications include certification and supervisory experience. Hiring location is in New Orleans, LA.
Job Description
Clinical Research Coordinator
I, II & III
(Covington, LA)
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, 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. 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 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
