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and regulatory submissions Provide input to the Statistics Group Lead to plan support for assigned studies and submissions. Communicate and collaborate with other project statisticians within the unit
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, Programming, Data Management). KEY RESPONSIBILITIES Provide scientifically rigorous statistical input into study design, statistical analysis plans, interpretation of statistical results, project development
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Experience with other statistical software (e.g., Stan) Programming experience (e.g., Python, C++) ORGANIZATIONAL RELATIONSHIPS Reports to Pharmacometrics Group Leader within the line organization of
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and regulatory submissions Provide input to the Statistics Group Lead to plan support for assigned studies and submissions. Communicate and collaborate with other project statisticians within the unit
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ROLE SUMMARY Will join a team of scientists supporting oncology development programs. Will be the Clinical Pharmacology Lead providing clinical pharmacology expertise to a multidisciplinary project
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to Statistics Program Lead and/or Statistics Therapeutic Area Head to plan support for assigned projects, studies, and submissions. Comply with all statistics and quality processes, Pfizer data standards
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. Experience in B2B and/or B2C marketing is a plus. BASIC QUALIFICATIONS: Bachelor ' s degree with 10+ years of experience OR master's degree with 9+ years of experience OR PhD with 7+ years of experience Degree
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resources to ensure all functional device activities are completed on schedule following the Pfizer Design Control process. Utilize technical writing and statistical data analysis skills to write protocols
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POSITION SUMMARY You will join a team of scientists supporting oncology development programs. You will be the primary Clinical Pharmacology Lead providing clinical pharmacology expertise to a
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+ year of experience, or PhD and 0-3 years of experience Degree in chemistry, biochemistry, chemical engineering, or related field Direct experience with antibodies, proteins, and/or bioconjugation Good