Clinical Research Coord I

Cooper University Hospital•Camden, NJ
•$25 - $43

About The Position

Assists the Principal Investigator and other members of the research team with preparing IRB protocols and consent forms and developing study budgets. Completes and maintains required study documents, assists with identifying and recruiting study participants, and works as a team player with everyone involved in the studies.

Requirements

  • 0–2 years of research experience.
  • High school diploma or equivalent required.

Nice To Haves

  • Medical Assistant, LPN, or Phlebotomist experience preferred.

Responsibilities

  • Assist the Principal Investigator and research team with preparation of IRB protocols and consent forms.
  • Assist with development of study budgets.
  • Complete and maintain study documents as required.
  • Assist with identification and recruitment of study participants.
  • Work collaboratively with everyone involved in the studies.
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