Clinical Research Coordinator (I, II, and III) - Full Time or Part Time

Job description

Clinical Research Coordinator (I, II, and III) - Full Time or Part TimeEpidemiology

Location: Morgan City, LA

Summary

The primary responsibility of the Clinical Research Coordinator is to manage all aspects of conducting clinical trials. The Clinical Research Coordinator is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for the protocol, the Clinical Research Coordinator acts as a liaison between the patient, investigator, Institutional Review Board and sponsor. The Clinical Research Coordinator screens, enrolls and follows study patients, ensuring protocol compliance and close patient monitoring, and works independently in designing, coordinating, and implementing all assigned research projects. The Clinical Research Coordinator is responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files.

Required Qualifications

The education required for each level is listed below:

Clinical Research Coordinator I (Pay Grade T2.23)

  • 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 T3.24)

  • 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 T4.25)

  • 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

 

 

 

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Job No:
Posted: 10/16/2019
Application Due: 11/30/2019
Work Type:
Salary: