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Clinical Research Coordinator I, II
1 month ago
Location:
Houma, 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 QualificationsThe 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 hireOR* 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 experienceOR* LPN with current state licensure at the time of hire and four (4) years of related work experienceOR* 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 experienceOR * LPN with current state licensure at the time of hire and five (5) years of related work experienceOR * 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
- Preferred Spanish language fluency-oral and written
- Preferred Spanish language fluency-oral and written
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