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The Senior Director of Real-World Evidence Biostatistics plays a pivotal role in leading and overseeing the strategic direction and execution of statistical and real-world evidence initiatives within the organization.
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SAS is the preferred statistical package within the HSS Biostatistics Program, but candidates with experience in other statistical packages (R, SPSS, Stata) are encouraged to apply. The Biostatistics and Bioinformatics Program in the HSS Research Institute seeks an MS-level Biostatistician, or equivalent, to provide comprehensive methodologic and analytic support to clinicians and basic scientists at the Hospital for Special Surgery.
$85,000 - $95,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Independently provides strategic statistical input to drug development planning, including feasibility assessments, development plans, complex/innovative study designs, novel statistical methodology, interpretations, regulatory submissions (NDA, MAA and JNDA) and follow up.
$220,000 - $260,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The Study Design and Biostatistics Center (SDBC) in the Division of Epidemiology and the Cancer Biostatistics Shared Resource at Huntsman Cancer Institute at the University of Utah invites applications for a faculty position at the Assistant or Associate Professor-level in either the Tenure or Research Track.
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In-depth knowledge of statistical methodologies, clinical trial design, and real-world evidence generation, with a focus on optimizing study design and data analysis. + PhD or MS (12+ years experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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MSc or PhD in Biostatistics or Psychometrics, or a relevant science, for example in Health economics, Public Health, Epidemiology, Pharmacoeconomics, or Psychology. The psychometrics team supports studies of instrument development, psychometric evaluation (classical and modern methods), and analysis of CObased study endpoints (e.g., longitudinal modelling, survival analysis, trial exploration, missing data & intercurrent event adjustment.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Represent the organization at conferences, forums, and industry events to showcase expertise and thought leadership in biostatistics and real-world data. Sr Director, RWE Biostatistics page is loaded.
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Responsible for managing relationships with CROs and other vendors for all study activities including study start-up, close out, and completion of Trial Master File. Responsible for collecting, preparing and reviewing regulatory documentation for IRB submission prior to study start-up.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Conduct data review, analyses, and interpretation of clinical trials data together with the GDL, Clinical Safety, and Biostatistics. Responsible for scientific leadership and execution of clinical studies and delivering on innovative clinical study designs, high quality trial execution, investigator engagement, data review, safety assessment, and interpretation of clinical study results.
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Identify and actively participate in relevant short courses, workshops, and seminars for further training (e.g., systematic reviews, biosafety, mass spectrometry) that is complementary to the postdoctoral fellow’s background and necessary for successful study execution.
$64,500 - $70,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Serve as the biostatistician in the Clinical Operations and Development team, responsible for all clinical study biostatistics deliverables. Solid understanding of drug development, clinical research, study design, pharmacokinetics, and medical terminology.
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Dragonfly Therapeutics seeks an Associate Director, Biostatistics to lead, develop, and implement statistical analyses to support our early development clinical trials, and provide support to investigators and researchers on experimental design and statistical approaches, requirements, and scientific standards.
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Provides ad-hoc programming support to Clinical Operations, Data Management, Statistical Programming, Biostatistics, Drug Safety, Clinical Science, Medical Writing and Drug Safety to ensure rapid access to clinical study data for data cleaning/validation, Clinical Data review, etc.
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The center continues to recruit independent investigators with expertise in diverse disciplines such as genomics, proteomics, immunology, medicinal chemistry, drug development, biostatistics and computational biology.
Part-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Take the computational biology lead on studies including; designing the study, the analysis plan and carrying out the statistical programming and data management to implement the plan. Ph. D. in Computational Biology, Biostatistics, Statistics, Bioinformatics or related field.
ExpandApply NowActive JobUpdated 9 days ago
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