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The Clinical Research Associate/Clinical Research Coordinator I (CRA/CRC I) works under general supervision to enroll eligible patients to clinical research protocols and manage all aspects of data collection and submission for multiple cancer studies.
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Hiring Manager is seeking a skilled Clinical Research Associate to oversee, manage and participate in research activities. Study Coordinator, Clinical Research Coordinator, Clinical Research Regulatory.
$30 - $35 an hourExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Experience 2-5 Years' experience as a Clinical Research Associate, Clinical Research Coordinator, Clinical Research Nurse Coordinator and proven experience as an Lead Auditor.
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This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace.
$50,000 - $100,000 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Research on Affective Disorders and Developmental Laboratory (Director: Dr. Roselinde Kaiser) is an interdisciplinary group performing clinical research to gain insight into the brain, behavioral, and developmental processes that reflect or underlie depression and other mood experiences, with the goal of leveraging our discoveries to foster emotional health.
$60,000 - $95,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Overview The Hemophilia Center, within the Institute of Development and Disability, in conjunction with the Division of Pediatric Hematology-Oncology (PHO), both within the Department of Pediatrics (DOP) and School of Medicine (SOM) at Oregon Health & Science University (OHSU), are seeking a pediatric hematologist with interest in clinical or educational scholarship at the assistant/associate professor level.
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Perform integrative analyses of multi-omics data from clinical trials and research cohorts, including genomics, transcriptomics, proteomics, and imaging, to identify biomarkers related to treatment mechanism and response, and potential therapeutic targets.
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Associate degree from an accredited college or university in chemistry, biology, biochemistry, cell biology or other natural, life, health care or materials science directly related to the research area to which the position is assigned and a minimum of three years' experience in a research, basic science or clinical setting particularly clinical trials research.
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Collaborate with translational scientists and clinicians to design and execute data analysis strategies that address key clinical oncology research questions. The base salary range for the Associate Director, Clinical Data Science - CEG is from :159,000-208,600.
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At least 7 years of experience in the pharma industry or clinical research institution is required. Develop and publish relevant bioinformatics methodologies, pipelines, and algorithms, and stay abreast of the latest advancements in bioinformatics, machine learning, and oncology research.
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The Clinical Data Science team at Eisai, Inc., is expanding its capabilities by acquiring in-house talent related to bioinformatics, machine learning, and big data analytics for the Oncology and Neurology clinical programs.
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Derive novel prognostic and predictive signatures using statistical and machine learning methods to guide patient stratification and biomarker selection in clinical trials. This position will be focused on the bioinformatics collaborations in Oncology clinical trials and will thus play a crucial role in analyzing large-scale genomic and clinical datasets to uncover insights into cancer biology and treatment response.
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Previous experience in oncology research is required. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development.
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Our core programs are supported by multi-disciplinary teams from hematology, medical oncology, surgical oncology, radiation oncology, pathology, radiology, research and bioinformatics, clinical operations, and dedicated clinical and support staff, including patient navigators.
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The Associate Research Compliance Officer (ARCO) will work under the oversight of the Dana-Farber Cancer Institute’s (DFCI’s, Institute’s) Research Compliance Officer (RCO) to grow and manage the activities of a high quality, robust, and sustainable research compliance program, with a focus on clinical research.
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