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Position Details Position Information Recruitment/Posting Title Clinical Research Coordinator (RCRC Clinical Study Manager I) Job Category Staff & Executive - Research (Laboratory/Non-Laboratory
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/or medical records. Assists with handling, processing, and shipping of biospecimens. Manage long-term archiving of biospecimens and correlating metadata. Thorough knowledge of the research study
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register consented research patients with study sponsor (e.g., industry, NCI Cooperative group, etc.) and inputs into the OnCore® clinical trials database maintained by the Cancer Institute of New Jersey
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to safe, effective study conduct; actively identifies and resolves obstacles in collaboration with the Principal Investigator (PI). Performs one-on-one or group protocol-related nursing education to
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to safe, effective study conduct; actively identifies and resolves obstacles in collaboration with the Principal Investigator (PI). Performs one-on-one or group protocol-related nursing education to
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to reduce ceramic cations as the raw material. The candidate is also expected to be well-versed in powder processing, processing in low Po2 environments, chemical and physical powder characterization
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study protocols; developing manuals of operations and training materials; preparing, submitting, and maintaining IRB documentation; coordinating with domestic and international collaborators; and
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study protocols; developing manuals of operations and training materials; preparing, submitting, and maintaining IRB documentation; coordinating with domestic and international collaborators; and
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. The Postdoctoral Associate will assist with scientific and operational aspects of ongoing studies. Responsibilities may include finalizing study protocols; developing manuals of operations and
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following: Recruits, consents, schedules and interviews study subjects. Collects quantitative and qualitative data from subjects and/or medical records. Creates and manages documents for Institutional