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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. ROLE SUMMARY This position will provide statistical support for
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business units. ROLE RESPONSIBILITIES Responsible for creating financial modeling, presentations, and market analysis to support contract decisions and Internal governance process: Run internal net cost
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May manage the study start up process in countries assigned (where SUPM not assigned) and/or oversee pCRO responsible for these activities as applicable Through the Site Care Partner/Country Trial
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therapeutic class, including competitor labeling, to help guide the team in developing labeling text. The GLL provides project management to the Labeling Team throughout the entire process, from the request
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. Analyze operational process problems and recommend appropriate corrective and preventative actions. Manage change control authoring and execution. Participate in the site and network wide teams to provide
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training slides and detailed information contained in the site Study Reference Manual. Provide support for queries and resolve issues from global study teams on the sample management process, including
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Sciences group by way of process improvement. Develop expertise navigating Pfizer compliance systems, registries (e.g. GDMS, pTMF, Clinical Trial Registries, etc.) and other study systems related
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. ROLE RESPONSIBILITIES Responsible for creating financial modeling, presentations, and market analysis to support contract decisions and Internal governance process: Run internal net cost models from both
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on deliverables throughout the process Provide input for the design of the Statistical Analysis Plan (SAP) and the clinical data output Responsible for review of patient level data across a study and for
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cutting edge design and process development capabilities to accelerate and bring the best - in - class medicines to patients around the world. What You Will Achieve In your role, you will be at the center