Assists the Principal Investigator and Sub-Investigators in coordinating all aspects of clinical research studies. Responsibilities include, but are not limited to: patient screening and recruitment; coordination of care of the research patient; protocol implementation; data collection and query resolution; device and drug accountability; submission to the Institutional Review Board (IRB); and assistance with account management of research study funds; correspondence with study sponsors and federal regulatory agencies for research; document preparation for site audits; and other related administrative and clerical tasks, as assigned.
Bachelor s degree or similar equivalent, required
Prior experience in healthcare institutions is strongly preferred
Two (2) years of cardiac research experience preferred.
Must have working knowledge of Microsoft Office products (Word, Excel, etcJob
Newark Beth Israel Medical Center is an Equal Opportunity Employer.
RWJBarnabas Health is an Equal Opportunity Employer