This position will provide statistical support for projects in the therapeutic area of Internal Medicine. The successful candidate will collaborate with study teams working effectively within the clinical triad (clinician, clinical pharmacologist, and statistician) to design studies, develop protocols, write statistical analysis plans, perform statistical analysis, write reports, present results summarizing findings, and develop publications of results.
Successful candidate would also participate in regulatory submissions and response to regulatory queries. The candidate will directly contribute to Company success by increasing the strength of study designs, interpretability of results, regulatory strategy & interactions, biomarker strategies and by implementing methods of model informed drug development. Additionally the candidate will work on methods development for application in but not limited to safety, benefit-risk, and study design.Responsibilities:
- Provide scientifically rigorous statistical input into project development plans, regulatory submissions and questions, interpretation of statistical results, study design, statistical analysis plans and scientific and commercialization projects.
- Be accountable for study level and submission level statistical deliverables on assigned projects, including timeliness and quality of deliverables according to project plans.
- Develop effective collaborations with others within clinical teams, partner lines (such as, Development Operations, Pharmaceutical Sciences, Safety Risk Management, Regulatory), and external regulatory, industry, professional and academic organizations.
- Ensure that all study and project level statistical activities are conducted in compliance with relevant regulatory requirements and Pfizer standards.
- Provide planning, delivery and communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta- analysis results, modeling and simulation in support of various activities, support for publications, scientific presentations, and support to product defense.
- Participate in research on statistical methodology and its applications pertinent to the Pfizer business needs.
- Help maintain a strong statistics community at Pfizer through collaborations, scholarship, presentations and learnings across divisions and locations.
- Advanced degree in statistics, biostatistics, or related field. M.S. in Statistics (or related field) with experience in applied statistics or Ph. D. in Statistics (or related field).
- Relevant experience providing an understanding of the processes associated with clinical, regulatory and marketing operations.
- Experience working with some of the following software, SAS, R, and Python. Candidates should have a reasonable level of comfort writing and working with statistical and data science related programming.
#LI-RemotePfizer requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Pfizer will consider requests for Reasonable Accommodations.Sunshine Act
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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.