Clinical Trials Coordinator II — Drive Protocol-Driven Research

Tulane group

New Orleans (LA)

On-site

USD 60,000 - 76,000

Full time

10 hours ago
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Job summary

Tulane University is seeking a Clinical Research Coordinator II to manage all aspects of conducting clinical trials in New Orleans, LA. The role requires in-depth protocol knowledge and adherence to good clinical practices, acting as a liaison between patients, investigators, IRB and sponsor.

The position involves screening, enrolling and following study patients under supervision, with data and regulatory file maintenance, including adverse event reporting.

Qualifications

  • Bachelor's degree or RN with current Louisiana state licensure at the time of hire and one year of related work experience
  • OR LPN with current Louisiana state licensure at the time of hire and four years of related work experience
  • Preferred qualification: knowledge of IRB submission process and requirements
  • Knowledge of good clinical practices as set forth by federal regulations

Responsibilities

  • Manage all aspects of conducting clinical trials.
  • Screen, enroll and follow study patients under supervision to ensure protocol compliance and patient monitoring.
  • Maintain data and source documentation and regulatory files, including adverse event reporting, under direct supervision.
  • Liaise between patient, investigator, IRB and sponsor to support trial activities

Skills

Protocol requirements
Good clinical practices
IRB submission knowledge

Education

Bachelor's degree
RN with LA licensure
LPN with LA licensure

Job description

Tulane University is seeking a Clinical Research Coordinator II to manage all aspects of conducting clinical trials in New Orleans, LA. The role requires in-depth protocol knowledge and adherence to good clinical practices, acting as a liaison between patients, investigators, IRB and sponsor.

The position involves screening, enrolling and following study patients under supervision, with data and regulatory file maintenance, including adverse event reporting.

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