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The Statistical Analyst B will use SAS, STATA, SQL, and/or R programming skills to develop and execute analysis plans, conduct sample size calculations, assist with database development, and develop and generate reports and projections to support study management and overall operations.
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Leads statistical programming efforts for BLA, MAA and other regulatory submissions, including SDTM and ADaM datasets and associated define files, tables/figures/listings for integrated summaries (ISS and ISE), etc.
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This is a postdoctoral position with the scientific goals being the development, implementation, and evaluation of statistical methods for causal inference based on electronic health records (EHR) data.
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In addition, the Principal Statistical Programmer works with management to delegate tasks appropriately, track progress, and provide expert technical support to team members. The Principal Statistical Programmer is a designated member of clinical sub-teams in the role of project lead Statistical Programmer.
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The Statistical Programming Group within the Department of Data Science is responsible for developing software for the analysis of clinical study data in accordance with departmental SOPs and guidelines.
$144,000 - $189,000 a yearRemoteExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Experience as a Statistical Analyst. SAS and / or statistical programming experience; Knowledge of statistical methods commonly used in pharmaceutical clinical trials. Write statistical programs for use in creating analysis datasets, tables, listings, and figures.
$80 - $100Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Demonstrated problem-solving, analytical, and multitasking skills with a good understanding of clinical research, statistical programming and CDISC standards. A technical and innovative role that partners with statistical programming, clinical analytics, data standards, statistical sciences, data sciences and information technology experts to implement next generation clinical data analysis ecosystem.
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The Associate Director of Quantitative Science is a self-sufficient and high-impact position that focuses on supporting the statistical and data science needs in the risk-based monitoring (RBM) of clinical trials, serving in roles such as CSM lead (CSM: Centralized Statistical Monitoring), while also support other activities such as preclinical studies, biomarkers, application of AI/ML and development of analysis applications.
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We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Medpace offers the following benefits for eligible positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, and pet insurance.
$65,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Discounts on local sports games, local fitness gyms and attractions. Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
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Lead the statistical programming activities for regulatory submissions following CDISC standards. Hands-on statistical programming for CSR, publications, presentations, DSUR, IB, safety data review, and ad hoc analyses.
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Main responsibilities:As a Senior Statistical Project Leader (Director) in our Statistical Innovation Hub, you will serve as the expert lead statistician in digital biomarkers for defining novel digital endpoints or re-engineering existing endpoints from digital Clinical Outcome Assessments (COAs.
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As part of ongoing transformation, integration, and restructuring efforts, we run various programs focused on reducing costs and improving margins.
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We're looking to speak with individuals that have experience working within the MFT Equities Trading space - with a preference for individuals with applied alpha research and statistical arbitrage strategy development experience.
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Overview Medpace is a full-service clinical contract research organization (CRO).
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Title: statistical Company: Nielseniq
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Operations Job Titles for Entry, Mid, and Senior-Level Positions
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Doing a job for eight hours a day, five days a week is exhausting for anyone. But for those with a disability or chronic pain, it can be especially taxing—something must change. Asking for reasonable accommodations at work can feel tricky, especially if you’re new to the job. Under the Americans with Disabilities Act (ADA), physical disabilities, health conditions, and symptoms of mental health are all valid workplace accommodations. When you request accommodations, it means that your condition is impacting your ability to perform at work.