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Oversee all EDC,and IRT vendor contracts for assigned clinical trials. AbbVie Data Science is the best-in-class team within its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data.
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Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for real-world evidence studies or clinical trials (e.g., ISO, MDD/MDR, CFR) The Data Scientist – RWE will be responsible for generating Real-World Evidence (RWE) through advanced analytics and innovative approaches in the clinical trials space.
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There is an exciting opportunity within the Precision Medicine Biomarker Program Management (BPM) group at AbbVie. The Precision Medicine group uses advanced methods to discover biomarkers for use in clinical trials.
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Manage and maintain vendor budgets for assigned clinical trials and process flows and data exchanges with global pharmacovigilance for clinical trial serious adverse events. Response Technology (IRT) vendors for assigned clinical trials.
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The redeveloped campus provides access to primary, specialty and emergency care, as well as a seamless pathway to specialty care from throughout the Northwestern Medicine network, including leading-edge clinical trials.
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Hospital paid retirement plan and tax-sheltered annuity plan About the Termeer Center Seeking an experienced oncology RN for this 22-chair clinical trials research unit specializing in first-in-human, Phase 1 Clinical trials.
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Education and/or Experience Combination: The Medical Technologist (Advanced Staff Technologist) must meet at least one of the following requirements below:(a) A bachelor's degree or higher from an accredited college or university in medical laboratory science, medical technology, clinical laboratory science or in a related science (e.g., laboratory sciences such as chemistry, biochemistry, biology, microbiology, immunology, etc.
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The Manager, Patient Experience Data & Strategy role within the Patient-Centered Outcomes Research (PCOR) team works independently while under the supervision of a Director to design and execute patient experience data (PED) evidence research to support optimization of product registration, access & reimbursement, and clinical practice in collaboration with HEOR Strategy and other functions (e.g., Clinical Development & Operations, Regulatory, Commercial.
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Line Staffing is now hiring Urgent Care LPN (Day shift).
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Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise.
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This position reports to the Medical Epidemiologist and works with the STI Program Coordinator to achieve clinical and practice goals set by the LCHD/CHC, Centers for Disease Control and Prevention (CDC), Health Resources and Services Administration (HRSA), and the Illinois Department of Public Health (IDPH.
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Review identified or anticipated technical or data related issues arising in the design, conduct or analysis of clinical trials or other scientific research. Provide statistical expertise for design, analysis and reporting of clinical or scientific research studies or programs and contribute to development of modern program/trial design methodologies with a focus on real world evidence (RWE) gathering, analysis and interpretation.
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Within the last ten years as a certified Medical Laboratory Technician by the American Society for Clinical Pathology Board of Certification (ASCP-BOC), American Society of Clinical Pathology Board of Registry (ASCP-BOR) or American Medical Technologists (AMT.
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With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
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Leads development & integration of COA measurement strategy into clinical development programs through clinical trial program support (e.g., protocol/SAP content development, results interpretation and CSR development) and ensures appropriate implementation of COAs on eCOA platforms in global programs.
$48.4 an hourFull-timeExpandApply NowActive JobUpdated Today
clinical trials jobs Title: social in Lake Forest, IL
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