Pfizer
Statistician
Overview
In this role, you will provide statistical inputs to study designs, statistical analysis plans, interpretation of statistical results, project development plans, and regulatory submission strategies through effective partnership with lead project statisticians.
About Pfizer
At Pfizer, our mission is straightforward: empower healthcare decisions regarding the safe and appropriate use of medicines for patients. Your work will ensure that our evidence is scientifically robust, providing unbiased and medically necessary expertise to enhance health outcomes.
Requirements & Eligibility
- PhD with at least 1 year of statistical consultation experience
- Proven track record in delivering timely and high-quality statistical contributions and scientific reports for clinical trials aimed at regulatory submissions
- Deep knowledge of experimental design and cutting-edge technologies to enhance business processes
- Ability to identify, comprehend, and apply pertinent scientific literature
- Strong written and verbal communication skills for clear and effective dissemination of information
- Experience in developing and managing plans to achieve objectives
- Ability to operate independently in ambiguous situations and make decisions to resolve moderately complex problems
Key Responsibilities
- Through effective partnership with lead project statistician, provide statistical inputs to study designs, statistical analysis plans, interpretation of statistical results, project development plans, and regulatory submission strategies
- Provide planning, delivery and communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, trial topline results, exploratory and meta-analysis results
- Support for publication activities, scientific presentations, and regulatory query responses
- Make decisions to resolve moderately complex problems, developing new options guided by policies in non-standard situations
- Develop effective collaborations with cross-functions within Clinical R&D, and external regulatory, industry, professional and academic organizations
- Accountable for study level and submission level statistical deliverables on assigned projects
- Collaborate with project statisticians and statistical leaders to establish consistent methodologies within the therapeutic area
- Ensure that all study and project level statistical activities are conducted in compliance with the company processes and relevant regulatory requirements
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