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practices. Provide scientifically rigorous statistical expertise on: Projects and protocols in support of clinical development and for publication, presentation, access negotiation, and other evidence
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(director/Sr director) provides clinical input to protocol/study team for monitoring guidelines, statistics analysis plans, ICDs, clinical review forms, data edit checks, data quality planning, as needed
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thinking and confident decision-making in building Pfizer's PCT capabilities. Support the Head of GME in establishing a PCT CoE. REQUIRED QUALIFICATIONS Doctorate (Ph.D.) in Public Health, Statistics, Data
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research processes, safety or regulatory requirements. Multitasking - Demonstrated ability to effectively work on simultaneous projects/deliverables. Analytical and Statistical Skills - Demonstrated
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problems. Proficient in statistical analysis. PREFERRED QUALIFICATIONS Solid background in virology, antiviral drug discovery, molecular biology, cell biology, and immunology, with practical working
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in the glucocorticoid and Hospital portfolio. Develop and support the dissemination of accurate, current medical and scientific knowledge (e.g.: disease states, product label, statistics interpretation
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in the glucocorticoid and Hospital portfolio. Develop and support the dissemination of accurate, current medical and scientific knowledge (e.g.: disease states, product label, statistics interpretation
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, statistics analysis plans, ICDs, clinical review forms, data edit checks, data quality planning, as needed (ultimately oversees work of protocol/study team). Contributes to contract research organization
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, statistics analysis plans, ICDs, clinical review forms, data edit checks, data quality planning, as needed (ultimately oversees work of protocol/study team). Contributes to contract research organization
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apply deep medical and clinical knowledge to translate clinical research ideas into high-quality decision-making data, working closely with subject matter experts from statistics, clinical pharmacology