Clinical Data Coordinator - Phase I Oncology
Current- Responsible for the accurate and timely sourcing and data entry of required clinical trial data into data capture systems and/or case report forms and ensures study compliance for all research participants within an assigned division.- Data management including review of source and electronic clinical programs to enable comprehensive data review, entry and cleaning data clarifications/queries within study specific timeframes.- Assures timely submissions of research data, laboratory specimens and query correspondences to all research affiliates and statistical centers.- Ensures that electronic databases contain accurate, complete and up to date records of each patient participating in a clinical trial.- Works collaboratively with research team members including but not limited to Principal Investigators, Research Nurse Coordinators, Sponsors, Contract Research Organizations and employees of Hackensack University Medical Center.- Organizes and prepares for all study related visits including site initiation activities, routine monitor visits, close-out visits, internal audits and sponsor audits.- Maintains adequate inventory of research supplies, and safely disposes of expired study supplies.- Prepares, processes and ships human specimens and biologic agents per protocol guidelines and federal regulations.
