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Role Summary
Manager, Statistics
Responsibilities
Provide statistical input into clinical study design and statistical analysis plans.
Ensure high-quality statistical deliverables are completed according to study timelines.
Ensure all statistical activities comply with regulatory requirements and Pfizer standards.
Develop data presentation plans, interpret statistical results, and contribute to clinical trial reports.
Support publications and scientific presentations of study results.
Collaborate with other project statisticians to ensure consistency in statistical approaches across studies.
Identify opportunities to apply innovative statistical methodologies to streamline development and support decision-making.
Participate in research on statistical methods relevant to PfizerβΓΓ΄s business needs.
Contribute to a strong statistics community at Pfizer through collaboration, knowledge sharing, presentations, and process improvement initiatives.
Qualifications
M.S. in Statistics, Biostatistics, or a related field with a minimum of 2 years of applied statistical experience; or Ph.D. in Statistics, Biostatistics, or a related field.
Strong verbal and written communication skills.
Solid understanding of statistical theory and its practical application.
Proficiency in SAS or R programming.
Ability to clearly explain statistical concepts to non-statistical colleagues.
Demonstrated ability to work collaboratively in a team environment.
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
Skills
Statistical modeling
Clinical trial analysis
Data interpretation and presentation
Collaboration and teamwork
Communication of complex concepts to non-specialists
Education
As above in Qualifications (M.S. or Ph.D. in Statistics/Biostatistics or related field).