NJ - Elizabeth (07202)
The Research Associate serves as a member of the clinical research team and provides research expertise in the day-¬to-day management of the clinical research program; including patient eligibility assessment, safety assessment, regulatory compliance, Institutional Review Board functions, and administrative issues involved in opening and maintaining industry, cooperative group and investigators initiated trials.
Certification through Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP), preferred. 2+ years experience in clinical research, preferably in an oncology setting. Study Coordinator certification (CCRC) are preferred with 2 - 4 years of experience in the oversight of oncology clinical trials. Computer knowledge, using Word, Excel, Power Point, Internet.