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of other colleagues to achieve meaningful outcomes and create business impact. Degree in Computer Sciences, Statistics, Clinical Informatics or similar Relevant certification &/or work experience in data
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of other colleagues to achieve meaningful outcomes and create business impact. Degree in Computer Sciences, Statistics, Clinical Informatics or similar Relevant certification &/or work experience in data
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team of an oncology program. ROLE RESPONSIBILITIES Acts as Clinical Pharmacology representative on Clinical Sub Team and Development Team, as appropriate. Provides the clinical pharmacology components
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analysis for multiple analyses supporting a program. Prepare formal presentations and written reports to Pfizer standards. Contribute to regulatory documents (summary documents, briefing books, regulatory
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to reduce care gaps, improve care efficiencies, and maximize quality and population health. Maintain, continually develop, and utilize clinical informatics capabilities to enable effective collaborations with
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Unit, which is focused on anti-tumor immunity and immune cell biology to support the execution and diversification of the Oncology Research pipeline. The incumbent will be an established scientific
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-Specific Document List algorithms to address rapidly changing business needs Manage investigator record retention program across Pfizer clinical trials Drive performance of CRO against TMF requirements
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management as it relates to driving labeling process in regulated industry MS Office Suite; expert formatting skills (Word, XML) Bachelor's degree (in science or life sciences preferred) Attributes: Knowledge
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utilized with full confidence in a compliant manner, these include: insights generation, field compensation, program performance calculation, SPP program performance, limited distribution network evaluation
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) Development and Oversight at disease area and program level including integration within the Quality Management System (QMS ), and ensuring individual asset and study level IQMPs are in place. Escalation