Pfizer Director Biostatistics, Nonclinical, Early Clinical Development in Pearl River, New York
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. S/he 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 vaccine assay specialists to support vaccine clinical and diagnostic assay development, qualification, and validation
Collaborate with vaccine preclinical scientists to support vaccine preclinical and nonclinical development
Ensure statistical rigor and good scientific practices are followed, excellent statistical methods utilized, and documented in protocols, analysis plans and manuscripts
Provide statistical expertise to regulatory submissions and ensure quality and appropriateness of submission deliverables
Bring innovative statistical thinking and methods to maximize the value of aggregate clinical and preclinical data in support of scientific and vaccine development strategies
Serve as a core member of scientific teams responsible for determining strategy and delivering results in a timely and high quality manner
Where possible, standardize processes and methodologies, may include developing statistical tools to aid scientists in standardized analyses.
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
PhD in Statistics/Biostatistics and at least 5-8 years of pharmaceutical experience or a MS in
Statistics/Biostatistics and at least 8-10 years of pharmaceutical experience
Strong pre-clinical and non-clinical experience is required
Must have strong technical competence, including statistical computing
Capability to provide statistical leadership to cross-functional teams.
Sound understanding of design of experiments, assay development, and statistical applications for preclinical research
Good knowledge of drug development regulations pertinent to statistical analysis
Assay validation experience, particularly clinical assays, is highly desired
Vaccine development experience is highly desired
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.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.
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Other Job Details:
Last Date to Apply for Job: December 1, 2018
Eligible for Relocation Package: yes
Eligible for Employee Referral Bonus: yes
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.