Bachelor Degree Facilitates clinical research activity at Moffitt Cancer Center and/or affiliated institutions by entering data on to case report forms (CRF’s), and/or register data using remote data entry and/or electronic data entry. Coordinator will also assist with new patient eligibility evaluation, registration, and coordinating protocol-related care of patients enrolled on clinical trials. The clinical trials coordinator is responsible for collecting all source documentation and worksheets prepared by all members of the research team and then transcribing the data onto the appropriate collection tool for submission to the sponsor. The clinical trials coordinator is knowledgeable of protocol requirements and good clinical practices as set forth by Federal regulations. Provides data management support for the various research protocols. Maintains the day-to-day flow of data and forms pertaining to clinical research. Act as a resource for program protocols, the coordinator will act as a liaison between the investigators, primary care providers, Moffitt regulatory staff and the sponsor.
Moffitt Cancer Center - 1 day ago - save job - block The H. Lee Moffitt Cancer Center and Research Institute, founded in 1986, is a National Cancer Institute-designated Comprehensive Cancer Cen...
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Cancer
Center
Clinical
COORD
Moffitt
Research
Tampa
COORD CLINICAL RESEARCH II - Moffitt Cancer Center - Tampa, FL
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