20 days old

Manager, Biostatistics

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+ Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices.

+ Provide statistical expertise and contributions for projects and protocols in support of clinical development.

+ Provide statistical expertise on regulatory submissions and ensure quality and appropriateness of submission deliverables.

+ Provide statistical expertise in maximizing the value of aggregate clinical data in support of scientific and drug development strategies.


+ Provide statistical input to study designs, statistical analysis plans, interpretation of statistical results, project development plans, regulatory issues and scientific and commercialization projects

+ Provide planning, delivery and communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results, support for publication activities, scientific presentations, and support to product defense.

+ Accountable for study level and submission level statistical deliverables on assigned projects.

+ Ensure that all study and project level statistical activities are conducted in compliance with relevant regulatory requirements and Pfizer standards.

+ Provide statistical input to cross-functional activities - collaborate with other statisticians, study managers, and other colleagues - for assigned studies and regulatory submissions

+ Ensure timeliness and quality of statistical deliverables according to project plans for assigned studies and projects.

+ Comply with all statistics and quality processes and standards that are applicable to statistical outputs, and support processes that require statistical input.

+ Communicate and collaborate with other project statisticians within the therapeutic area to ensure consistency of statistical approaches

+ Participate in technical forums on statistical methodology and its applications pertinent to business needs.

+ Help maintain a strong statistics community at Pfizer through collaborations, scholarship, presentations, and learnings across divisions.


+ Advanced degree in statistics, biostatistics, or related field.

+ Capability to provide statistical leadership to cross -functional teams at the protocol level.

+ Strong statistical skills with application to clinical trials and/or analysis of observational studies

+ Effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization.


At least 4 years of relevant clinical trial and business experience


Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Posted: 2020-05-05 Expires: 2020-06-05
Sponsored by:
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