18 Statistics positions at Pfizer in New-York in United States

Associate Director, Biostatistics

practices. Provide scientifically rigorous statistical expertise on: Projects and protocols in support of clinical development and for publication, presentation, access negotiation, and other evidence

Manager, Biostatistics

-functional teams to provide effective statistical consultation with scientists and toxicologists. You will collaborate with scientific colleagues across a diverse set of disciplines in DSRD, on the design

Associate Director, Biostatistics

-functional teams to provide effective statistical consultation with scientists and toxicologists. You will collaborate with scientific colleagues across a diverse set of disciplines in DSRD, on the design

Senior Manager, Data Science and AI

across various fields, our team leverages advanced statistical analysis, machine learning techniques, and data visualization tools to uncover patterns, trends, and correlations within the data

Associate Director, Clinician, Medical Monitor - Vaccines (MD required)

(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

Sr. Director, Pragmatic Clinical Trials Clinician (Non-M.D.)

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

Document Quality, Manager

research processes, safety or regulatory requirements. Multitasking - Demonstrated ability to effectively work on simultaneous projects/deliverables. Analytical and Statistical Skills - Demonstrated

Associate Research Fellow, Anti-Infectives

problems. Proficient in statistical analysis. PREFERRED QUALIFICATIONS Solid background in virology, antiviral drug discovery, molecular biology, cell biology, and immunology, with practical working

Director, Clinical Monitor, Vaccines (MD required)

, 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

Director, Clinical Monitor, Vaccines (MD required)

, 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