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Under the Director of Clinical Trials and the direct supervision of the Clinical Research Nurse Manager, coordinates and manages clinical trials in accordance with federal and state regulations, Institutional Review Board (IRB) approvals and Connecticut Children's policies and procedures.
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The Clinical Research Nurse I serves as Clinical Research Nurse 1 for phase I, II and III oncology clinical trials conducted in the Lombardi Clinical Trials Office (Lombardi CTO) at Lombardi Comprehensive Cancer Center.
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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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Faculty regularly publish in the top methodological journals across all major biostatistical research areas, including causal inference, clinical trials, statistical genetics, bioinformatics, genomics and proteomics, analysis of spatial and longitudinal data, biomedical imaging, survival analysis, meta-analysis and data synthesis, and mobile health.
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The Director, Clinical Data Management will be responsible for daily data management tasks for all phases of clinical trials including CRO oversight and support other functional areas such as clinical operations, statistical programming, biostatistics, and medical monitor.
$242,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Act as a liaison with hospital staff, physicians, IRB, review committees, clinical research finance team, and auditors; Act as a liaison with sponsors during study start-up activities and participate in site initiation visits, monitoring visits, and audits.
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Walgreens RWE Real World Evidence Clinical Trials is seeking an Account Director, RWE Clinical Trials with proven business development, client management, and stakeholder management skills to drive the success of the Walgreens RWE Clinicals Trials business segment.
$222,500 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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HJF is seeking a Regulatory Compliance Specialist - Clinical Trials to assist in the compliance of HJF research programs with applicable local, state and federal regulations for human subjects research, animal use research, genomics/proteomics, and Health Insurance Portability and Accountability Act (HIPAA.
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This new joint venture will establish a fully integrated oncology research organization aimed at expanding clinical research, accelerating drug development, and increasing availability and access to clinical trials for community oncology providers and patients, including those in underserved communities.
$228,400 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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The Clinical Data Coordinator must be able to review clinical trial protocols and understand inclusionary and exclusionary criteria for clinical trials. 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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Within his first three years, with sharply more robust clinical trials activity, Ohio State became the 37th full voting member of RTOG. Further, in 2022, Ohio State Radiation Oncology rose to #1 in NRG Oncology clinical trials accrual in the United States, according to NCI-CTEP data, keeping up with the increase in clinical volume.
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Sarah Cannon Research Institute (SCRI) is one of the worlds leading oncology research organizations conducting community-based clinical trials. It has conducted more than 750 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA today.
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The Clinical Research Supervisor reports to the Research Administrator, Clinical Trials Manager, Research Vice Chairs and works directly with Principal Investigators within the Department of Obstetrics, Gynecology and Women's Health on the execution of reproductive health research studies, focusing on protocol development and coordination, supervising research/study assistants, and data cleaning and monitoring.
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A Senior Research Scientist that specializes in organ transplantation and social behavioral science, chronic disease will work mostly with primary data collected through large multi-site studies and clinical trials in support of NIH and DoD funded research.
$150,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Analytical Skill, Analytical Skill, Analytical Thinking, Chemical Biology, Chemistry, Clinical Trials, Collaboration, Communication Skills, Curiosity, Data, Data Analysis, Design Of Experiments, Detail-Oriented, Drug Development, Drug Discovery, Ethics, Gene Therapy, Immunology, Inventory Management, Laboratory, Lifesciences, Machine Learning (Ml), Management, Medical Research, Molecular Biology {+ 10 more.
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clinical trials data review jobs Title: scientist Company: Nationwide
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