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The Radiologic Technologist is responsible for performing all Radiology exams and other clinical duties. Review and ensure exams are high quality and available for interpretation in a timely fashion.
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The Division of Medical Genetics seeks a Genetic Counselor to coordinate studies and clinical trials for genetic diseases, and provide genetic counseling to patients participating in various research studies and related settings.
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The Global Market Access team at Dexcom (comprised of Health Economics Outcomes Research (HEOR), Global reimbursement/Access, government affairs, and post-market clinical evidence planning) is responsible for identifying, planning, and executing post-market clinical and economic value studies and analyses, as well as establishing global healthcare system access for Dexcom's growing product portfolio.
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Demonstrated current competence and evidence of the performance and interpretation of at least 200 general radiology examinations, 100 CT examinations, 100 MR examinations, reflect of the scope of privileges requested, or successful completion of an ACGME or AOA accredited residency or clinical fellowship within the last 12 months.
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The Executive Director, Biostatistics has extensive experience in the pharmaceutical industry to independently lead a therapeutic area biostatistics team (e.g. Neurology, Metabolics, Hematology/Nephrology, Metabolism or other) to deliver project, tools and/or technical level activities related to design, delivery and interpretation, advises statisticians across business units to prepare for high level internal governance committees and/or regulatory submissions.
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The Chair will be responsible for the assurance of excellence in community engagement, education, and research within the Department of Obstetrics and Gynecology, as well as for partnership with health system leaders in the delivery of top-quality clinical care.
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Work with statisticians/biometrics to develop the required tables/listings/figures and contribute to the interpretation of efficacy and safety data from clinical trials. in science is required, and 3+ years of experience in clinical research and/or drug development within the pharmaceutical industry.
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Proven experience in the design and conduct of pre-clinical and non-clinical metabolite profiling and characterization studies including structural elucidation, interpretation of mass spectra and determination of metabolic pathways.
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Represent the Real World Evidence function and collaborate with internal and external stakeholders in the analysis and interpretation of clinical real world studies. Able to effectively present research results to study team and other collaborators, including results interpretation and drawing appropriate inferences based on study design/statistical methods as well as assessment of study limitations.
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As a Director of Biostatistics, you will assume a prominent role in leading a diverse range of projects, offering expert consultation and collaboration with professionals in epidemiology, informatics, clinical, data science, and engineering.
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We offer stimulating and rewarding careers in a wide array of disciplines: SPED Educators, Behavioral and Mental Health, Sign Language Interpretation, and more. 1 year of verifiable, professional experience as a Physical Therapist within the last 3 years (may include residency or clinical practicum.
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Serve as an individual contributor and senior-level representative of Precision Medicine on development teams to integrate, influence and deliver biomarker strategies to key programs from initial concept to execution, data delivery and results interpretation.
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The Medical Director provides medical interpretation and determinations whether services provided by other healthcare professionals are in agreement with national guidelines, state and CMS requirements, Humana policies, clinical standards, and contracts.
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Ensures the medical review and interpretation of efficacy and safety data from clinical trials; this includes delivery of top-line report in collaboration with study statistician, and delivery of clinical study report in collaboration with medical writer and accountable for overall quality and timeliness of analysis and reporting are conducted appropriately.
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Reports shall include deliverables documenting all neuropsy-chological and psychological tests administered, individual performance on the tests as compared with normative data, interpretation of the data based on best practices in the neuropsychology field, and numerical test data for individual patients.
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