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 projects as needed or assigned.
Ensures proper research billing in EPIC.
Is flexible and can adapt to the changes healthcare is experiencing.
Assists with the identification and recruitment of study participants.
Work as a team player with all involved in the studies.
Additional duties as assigned by manager.
Minimum 3-5 years of research experience required.
High School Diploma or GED required
Bachelors Preferred
Basic understanding of Microsoft Excel, Outlook and Word.
USD $29.00
USD $48.00
Clinical Research Coordinator II • Camden, NJ, United States
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