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The Community Practice Clinical Data Coordinator at Trial Library will play an integral part in expanding access to cancer clinical trials by pioneering pre-screening efforts in community oncology settings.
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May perform any of the following depending on work location: specimen accessioning and data verification; specimen handling and transport to facilitate clinical testing and clinical trials; performing laboratory or equipment maintenance; maintains inventory of various laboratory and operating supplies.
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Performs gating, analyses and scientific review of high dimensional flow cytometry data collected from immuno-oncology clinical trials. Must have at least 5 years of experience in analysis of high dimensional (12+ color) flow cytometry data, specifically with T-cell functional subsets (memory, activation, exhaustion) and/or Myeloid cell phenotyping (MDSC, pDC etc.
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Coordinate the day-to-day execution of clinical trials, with a focus on site start-up, patient enrollment, monitoring, and data flow metrics from clinical sites, clinical research organizations (CROs), and central labs.
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Previous experience working in a matrixed environment to implement flow cytometry assay development and validation to support clinical trials. In this vital role you will design, develop and implement clinical biomarker assays employing innovative flow cytometry methods and techniques to support our drug development efforts.
$138,904 - $165,489 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Collaborate with various functions to ensure robust CRF/EDC development, and quality data collection for the assigned clinical trials. Principal Data Scientist: Biostatistics will report to the VP, Data Science and will focus on providing strategic input and technical expertise on statistical methodology to support the research and development organization for assigned projects They will participate as active members of a cross-functional team to plan, lead and execute the tasks required to support the clinical development for the assigned programs.
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Management, development, and execution of the financial IT systems and data within the CTO.Develops and implements financial policies and procedures for the CTO.Assesses financial data security and management practices in the CTO.Ensures compliance with government and University rules and regulations relating to financial aspects of Clinical Trials.
$110,000 - $135,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The DIR clinical research program performs clinical research that leads to a better understanding of biology and clinical pathology, ranging from first-in-human clinical research trials to natural history studies of rare disease processes.
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Oversee and ensure quality control of the pathology team’s methods and data from internal and external labs to support primary, secondary and exploratory endpoints in clinical trials under regulated approaches (GLP, GCP.
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ABOUT THE JOB: Summary:The Clinical Research Coordinator may coordinate device and drug treatment research trials, as well as observational studies conducted at Children's Medical Center, including but not limited to study set-up, implementation, fiscal monitoring, and data collection/entry.
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Technical expertise in immunology, biomarker discovery and development in clinical trials, including assay development, validation, and data analysis. Execution: Work closely with cross-functional teams to design and execute biomarker-driven clinical trials.
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The research trials may include treatment trials, biomarker trials, imaging trials, neurocognitive and motor control studies and other research. IRB review process, informed consent, trial design, data monitoring as well as good writing and editing skills a plus.
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Our physicians are also actively involved in clinical research and conduct many clinical trials, including those in conjunction with NIH-sponsored groups such as RTOG (Radiation Therapy Oncology Group.
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In oncology, the rapid development and deployment of increasingly sophisticated molecular assays has created an unprecedented scale of biomarker data for patients in clinical trials.
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Provide guidance in interpreting the data from pharmacometric analyses, including PPK, exposure-response analyses, and other quantitative analyses, to recommend dosing paradigm for different phases of clinical development; provide justification for dose selection for pivotal clinical trials.
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clinical trials data jobs Company: Boston Pharmaceuticals
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