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Our ideal candidate would be an early to mid-career medical oncologist focused on thoracic malignancies with leadership skills to help drive the growth and visibility of our multidisciplinary program here at Mayo Clinic AZ. The successful candidate will be able to partner with our internationally recognized surgical, medical, and radiation teams in a multidisciplinary clinic; initiate, run and develop clinical trials; recruit future colleagues and drive innovation across the spectrum of care.
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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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We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida.
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The practice offers Hematology/Medical Oncology, Radiation Oncology, Palliative Care, and Clinical Trials & Research Programs. Ability to Enroll Patients in Clinical Trials.
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Coordinate patient care activities and participate in the conduct of studies for patients enrolled in clinical trials for multiple services including medicine and radiation oncology, etc.
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Analyze unstructured and/or structured biological data from biosensor clinical trials and evaluate biosensors performance to support product designs. This Sr. Engineer role supports our next-generation biosensor product design and development, focusing on clinical data analyses and sensor algorithm verification and improvement.
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Designs and facilitates implementation of the clinical biomarker strategies for company-sponsored clinical trials. Expertise in a relevant platform technology (immunohistochemistry, digital pathology, flow cytometry, or genetics), including assay development, data analysis, and clinical application, is required.
$201,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The oncology clinical research nurse I is expected to develop and maintain competencies in clinical research nursing in the first year of the position including but not limited to comprehension and compliance with all NYU PCC Clinical Trials Office policies and procedures, NYU OSR and IRB policies and procedures, familiarity and application of Good Clinical Practice (GCP) guidelines and Federal Regulations that govern the conduct of human subjects research.
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Oversee all EDC,and IRT vendor contracts for assigned clinical trials. Manage and maintain vendor budgets for assigned clinical trials and process flows and data exchanges with global pharmacovigilance for clinical trial serious adverse events.
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Reporting to the Head of Clinical Supply Chain, the Associate Director of Clinical Supply Planning will focus on managing and optimizing global supplies to ensure timely availability of clinical supplies for clinical trials.
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Experience drafting and negotiating clinical trial agreements. Experience with clinical trial and/or research agreements with ability to handle increasing levels of responsibility. Support strategic initiatives of the VP/ Deputy General Counsel and EVP/ General Counsel.
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Leading research: MultiCare Institute for Research & Innovation partners with our pediatric providers, offering ground-breaking research and clinical trials. Together, we are creating an environment where nurses are owners in the clinical decision-making process, are well connected, have open communication with their colleagues, feel supported to develop professionally, and understand the future of nursing at MultiCare.
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Job Summary:The Sr. Clinical Research Coordinator within the Ophthalmic Clinical Trials and Translational Center (OCTTC) is responsible for managing, coordinating, and implementing all components of clinical research protocols, including pre and post-research activities both within and outside the clinical setting.
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Serves as a subject matter expert in immunoassay-based assay development and validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in clinical trials.
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Human Subjects' Research - As applicable, oversee the submission of necessary documents required by the NYU Institutional Board (IRB), NYU Office of Clinical Trials and any other appropriate parties in order to obtain approval to conduct human subjects research (e.g., ensures the update and submission of necessary documents and/or forms to appropriate destination.
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clinical trials jobs Title: oncologist Company: Mayo Clinic
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