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As The Director, Statistical Programming, you will be a champion of Otsuka's culture and values and serve in a leadership role within the Statistical Programming group.
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Reporting into the Senior Director, Statistical Programming, the Associate Director, Statistical Programming will be responsible for supporting Clinical Development programs by performing Statistical Programming tasks as well as building and computing the analytical programming environment.
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The Associate Director, Statistical Programming will also assist with development of statistical programming processes and workflows. The Associate Director, Statistical Programming will be responsible for leading statistical programming activities for multiple clinical studies ensuring timely deliverables with high quality and coordinating with external statistical programming FSP. Successful candidates will oversee the quality and management of CRO’s work, as well as collaborate regularly with internal stakeholders.
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As the Director, Statistical Programming, the person in this position will provide statistical programming expertise and leadership for the function, and will be responsible for developing and maintaining Statistical Programming processes, standards and systems, planning and managing statistical programming resources to meet business needs across all clinical programs, and playing a key role in oversight of statistical vendors.
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In close collaboration with the Head of Statistical Programming & Clinical Data Science, you will shape strategies surrounding DM vendor oversight, process automation, and the implementation of cutting-edge technologies.
$224,000 - $233,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Director: 10+ years Statistical Programming exp in biotech/pharma/CRO, including 5+ years managing programmers & overseeing outsourcing. statistical programming function within the Biometrics department.
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Lead and manage external (and/or internal) biostatistics and statistical programming resources supporting studies and programs. He/She is also accountable for the production of biostatistics deliverables by providing oversight of the work performed by CROs, managing external (and/or internal) biostatistics and statistical programming resources, or performing the work themselves.
$220,000 - $260,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Associate Director, Statistical Programming for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.
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Bachelor’s or higher degree in Computer Science, Mathematics, Physics, Quantitative Finance, Engineering, Statistics or equivalent field, with significant coursework or equivalent experience in programming, modeling, simulation and statistical techniques.
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As the Director, Statistical Programming you will lead the Statistical Programming function for our clinical development programs at Larimar, contributing to the vision, direction, and strategy of the statistical programming function and of Statistical and Quantitative Sciences (SQS) as a whole.
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Hands-on professional programming experience across power industry and power trading is a big plus. Manage, troubleshoot and enhance trading models, data collectors and data stores leveraged by FTR trading team across transmission power flows, power generation economic dispatch, automated monitoring, analysis of transmission system constraints and statistical simulation based on historical data.
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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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ROLE SUMMARYProvide statistical leadership and technical support for Pfizer projects involving health economics and outcomes research (HEOR). The applicant is expected to develop highly effective collaborations with relevant stakeholders including those in Patient Health & Impact, the Patient-Centered Outcomes Assessment Group, Statistics, Clinical Pharmacology, Clinical Development, Medical Affairs, Epidemiology, Programming, and other groups contributing to HEOR analysis and strategy.
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Reporting to the Head of Statistical Programming, the Associate Director is responsible for the planning, execution, and quality of SAS programming to conduct statistical analyses in support of clinical trial results.
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Enhance statistical expertise in value-based drug development among Pfizer HEOR scientists, statisticians, and clinicians through active engagement and leadership in research methodology and content-specific areas.
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