Department: LCCC - Clinical Trials - 426806
Vacancy ID: P009330
Position Summary: WHEN APPLYING TO THIS POSTING YOU WILL BE APPLYING FOR THE FOLLOWING TWO POSITIONS: 20011692 & 20011693. This position serves as a Study Coordinator in the UNC Lineberger Comprehensive Cancer's Oncology Clinical Protocol Office. The primary responsibilities include: the informed consent process, eligibility and screening, toxicity assessment, patient management, conducting in-services for nurses staff in treating clinic; planning of patient recruitment methods; logistics of patient visits; logistics of obtaining and coordinating clinical samples; specimen collection as needed, enlistment of support of necessary ancillary departments; coordinating the ordering of the required supplies; preparation of study tubes, collecting source documentation; Data entry / management for assigned studies, working with Clinical Research Associates to facilitate data collection for CRFs (case report forms) and/or eCRFs for trials as assigned; prepare and participate in monitoring visits; facilitate pre-site meetings, site initiation meetings, and plan, organize and run protocol start-up meetings.
Application Deadline: 11/29/2018
Qualification and Experience: Licensed to practice as a Registered Nurse in the State of North Carolina and two years of experience in the area of specialization.
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