Clinical Research Coordinator II

Cooper University Health CareCamden, NJ
42d$28 - $46

About The Position

Assists the research manager, principal Investigator, and other members of the research team with preparation of IRB protocols, consent forms, data entry, and other tasks as needed. Completes and maintains all study documents as required. Assists with the identification and recruitment of study participants. Work as a team player with all involved in the studies.

Requirements

  • Minimum 3-5 years of research experience required.
  • Basic understanding of Microsoft Excel, Outlook and Word.

Nice To Haves

  • Bachelors Degree preferred

Responsibilities

  • Assists the research manager, principal Investigator, and other members of the research team with preparation of IRB protocols, consent forms, data entry, and other tasks as needed.
  • Completes and maintains all study documents as required.
  • Assists with the identification and recruitment of study participants.
  • Work as a team player with all involved in the studies.

Benefits

  • health
  • dental
  • vision
  • life
  • disability
  • retirement
  • opportunities for career growth through professional development
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