Clinical Research Coordinator II, COVID-19 Study

Job description

Clinical Research Coordinator II, COVID-19 StudyEpidemiology

Location: New Orleans, LA

Summary

The primary responsibility of the Clinical Research Coordinator II is to manage all aspects of conducting epidemiological research studies. The Clinical Research Coordinator II is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As one of the primary resources for the protocol, the Clinical Research Coordinator II acts as a liaison between the patient, investigator, collaborators, Institutional Review Board and sponsor. The Clinical Research Coordinator II is able to recruit, screen, enroll and follow study patients, and perform the associated data collection, entry, and quality control activities, under supervision, ensuring protocol compliance and close patient monitoring, continuing the required learning process record in this second level position for advancement towards a Clinical Research Coordinator III position. The Clinical Research Coordinator II is responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files, under direct supervision. The Clinical Research Coordinator II may also perform simple procedures , as well as laboratory processing, as called for by the study protocol(s). The Clinical Research Coordinator II will conduct and oversee staff training as required, assist the senior program manager with the supervision of staff and research assistants and manage the distribution of study outreach materials and compensation. 

Required Qualifications

  • 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 a Master’s degree in a related field

Preferred Qualifications

  • Knowledge of IRB submission process and requirements.  
  • Knowledge of good clinical practices as set forth by federal regulations.
  • Experience in field research.
  • Proficient in SAS or SPSS.

 

 

 

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Job No:
Posted: 11/10/2020
Application Due: 1/9/2021
Work Type:
Salary: