Clinical Research Coord I-PRN

Cooper University Hospital
Camden, NJ
Category Research
Job Description
Role Overview

Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, and development of study budget.

What You Will Do

Completes and maintains all study documents as required. Assists with the identification and recruitment of study participants.

Why It Might Be a Fit

Work as a team player with all involved in the studies.

Requirements

  • 0-2 years research experience
  • Medical Assistant, LPN or Phlebotomist experience preferred
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