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Experience and/or knowledge of the healthcare data domain in at least one of: electronic medical records (EHR/EMR), clinical imaging, clinical workflows; Electronic Data captures (EDC), and/or clinical research/trials.
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The Clinical Trial Manager in the Research Alliances team will oversee the planning, execution, management, and reporting of clinical projects supporting Iovance commercial activities, including expanded access programs (intermediate and single-patient) and Phase 4 post marketing pharmacovigilance studies.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Experience with clinical systems including various EDC, IRT, TMF, CTMS, etc. Manage the development of clinical protocols, amendments, informed consent forms,study plans and any other clinical research related documents, in collaboration withcross-functional team members or CRO-partners.
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Experience in Biostatistics, SAS programming, and clinical data management in a regulated clinical research environment. Develop and contribute to Biometrics SOPs and standard working documents meeting regulatory requirements throughout biometrics processes including IWRS/EDC, STDM, statistical programming for TLFs, and data reporting.
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Conduct Clinical Research Coordinator activities for assigned clinical research device studies including consenting participants, conducting study sessions, maintaining device accountability, and completing data entry into the Electronic Data Capture (EDC) system.
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Stanford University’s Department of Neurosurgery is seeking a Clinical Research Coordinator Associate (CRCA) to perform duties related to the coordination of clinical research studies.
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Participate in strategic planning and develop optimal clinical development plans with cross-functional drug development teams. Review and comment on eCRFs, annotated eCRFs, edit checks documents and other clinical data management related documents.
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Master's degree in statistics or biostatistics with 8+ years of biopharmaceutical statistics experience with specific experience in late stage drug development, including phase IIb, phase III, and submissions in the pharmaceutical industry.
$198,000 - $242,000 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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This role will support digital/wearable medical device clinical research studies conducted by Clinical Development that take place at the Verily Clinical Research Site in South San Francisco.
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Work with vendors to ensure that all study services comply with the study plan and budget; this may include clinical research organizations (CROs), electronic data capture vendors (EDC), and suppliers.
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