Clinical Research Coordinator II
US-NJ-Camden
External Career Portal
Req #: 72007
Type: Full Time
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Responsibilities: Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, and development of study budget. 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. Qualifications: Basic understanding of Microsoft Excel, Outlook and Word
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