Pfizer Associate Director Biostatistics in Cambridge, Massachusetts
A career at Pfizer offers opportunity, ownership and impact.All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.
Pfizer's ECD Statistics is looking for a motivated and experienced statistician with a solid background in nonclinical statistics, strong consulting skills, and an interest in collaborating with research scientists in drug discovery and development. He/She will work closely with research scientists seeking to discover new medicines in a variety of therapeutic areas by supporting the design and analysis of preclinical experiments covering all aspects of drug discovery from disease target identification, pharmacology studies, animal model development, biomarker development and demonstration of proof of concept. The focus will be on both "platform" approaches (ie ensuring robust assay methods) as well as specific project approaches. The ideal candidate will have a genuine interest in understanding drug target biology in order to provide effective statistical consultation with biological scientists.
Collaborate with preclinical scientists across research units (Immunology & Inflammation, Internal Medicine, Rare Disease, CTI) to design, analyze and present experiments. Bring innovative statistical thinking and methods to help drive the enhanced quantitative drug discovery and development paradigm within Pfizer.* Ensure rigorous approaches are taken to ensure good scientific practices are followed: excellent statistical methods utilized and documented in protocols, analysis plans and manuscripts, and assay methods are appropriately blinded, randomized and designed to meet clear objectives.Serve as a core member of scientific teams responsible for determining strategy and delivering results in a timely and high quality manner.Work with scientists to understand the biology and improve existing biomarkers, endpoints, derive new endpoints, and develop 'fit-for-purpose' statistical models.Use statistical expertise to prepare both internal and external reports, presentations and manuscripts, with the aim to improve the quality of internal decision making and increase our influence on the external environment.Where possible, standardize processes and methodologies within and possibly across therapeutic areas may include developing statistical tools to aid scientists in standardize analyses.*Provide statistical expertise on regulatory submissions and ensure quality of deliverables.
- PhD in Statistics/Biostatistics and at least 3-5 years of pharmaceutical experience or a MS inStatistics/Biostatistics and at least 5-8 years of pharmaceutical experience* Strong pre-clinical and non-clinical experience is required* Must have strong technical competence.* Capability to provide statistical leadership to cross-functional teams.* Sound understanding of design of experiments, assay development, and statistical applications for preclinical research* Interest in biology, graduate level training preferred.* Good knowledge of drug development regulations pertinent to statistical analysisPHYSICAL/MENTAL REQUIREMENTS:* Preferred candidates will have good computational skills in SAS, R, or S-Plus.* Strong communication skills and the ability to work collaboratively with research scientists are essential.* Demonstrated ability to work effectively as a part of a team.#LI-SA1
EEO & Employment Eligibility
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Associate Director Biostatistics Cambridge, Massachusetts 1051319-1852