Pfizer Senior Director, Biostatistics, Early Clinical Development in Cambridge, Massachusetts
Biostatisticians play a critical role in the advancement of new medicines at Pfizer. The right candidate will partner with senior management, clinicians, clinical pharmacologists, translational medicine, and other scientists to support early clinical development for Oncology.
The statistician will be involved in the design, execution, analysis, and reporting phases of clinical protocols and provide statistical expertise on regulatory submissions and ensure the quality and appropriateness of submission deliverables. She/he will support the development of innovative and efficient plans for developing new medicines in a variety of cancer indications. She/he will review scientific literature, promote innovation, efficient design and quantitative decision-making within research and in partnership with other lines, reducing the time and cost of drug development.
Core member of scientific teams responsible for determining strategy and delivering results in a timely and high quality environment.
Leader to bring innovative statistical thinking and methods to help drive the enhanced quantitative drug discovery and development paradigm within Pfizer. Central to this approach is the systematic review of prior information, statistical model building and simulation, utilizing Bayesian methods as appropriate, to design more effective studies.
Frequently interact with regulatory agencies regarding accelerated clinical development options for indications that have substantial unmet medical need.
In depth knowledge of more than one area of statistics, all commonly used, that enables to exert broad influence via advice to numerous project statisticians.
Leads initiatives to improve understanding and application of statistical methods
Strong insight into the Business needs and seek out areas where statistics adds most value, influencing others to ensure we focus our efforts on these key areas.
The qualified candidate must have a M.S. or Ph.D. in Statistics, Biostatistics, or related field, as well as a minimum of ten years experience in applying statistics in a pharmaceutical or related industry. Ideally, this experience would include exposure to the design and analysis of clinical studies in oncology early clinical development. The preferred candidate will have excellent statistical knowledge with the ability to apply this to scientific and clinical problems with experience in computational simulation, analysis of biomarkers, and Bayesian statistics. The preferred candidate will have a proven ability to manage multiple complex projects with a track record of influencing external environment through contributions to scholarship, working parties etc., as evidenced by committee membership, presentations and publications with demonstrated scientific productivity in advancing the state-of-the-art in applied statistical methodologies.
Strong communication skills with the ability to influence widely and work collaboratively with clinical project teams and senior management are required.
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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Additional Offer Details:
Last Date to Apply for Job: March 15, 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.