Clinical Research Coord I-PRN
Cooper University Hospital•Camden, NJ
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 all required study documents, assists with identifying and recruiting study participants, and works collaboratively with everyone involved in the studies.
Requirements
- 0–2 years of research experience.
- High school diploma or GED.
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 required study documents.
- Assist with identification and recruitment of study participants.
- Work as a team player with everyone involved in the studies.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
