Use Your Power fPurpose
At Pfizer, our mission is straightforward: empower healthcare decisions regarding the safe appropriate use of medicines fpatients. Your work will ensure that our evidence is scientifically robust, providing unbiased medically necessary expertise to enhance health outcomes. By investigating ways to close data gaps developing frameworks, you will contribute to the safe appropriate use of medicines fpatients, making a significant impact on global health.
What You Will Achieve
In this role, you will:
● Through effective partnership with lead project statistician, provide statistical inputs to study designs, statistical analysis plans, interpretation of statistical results, project development plans, regulatory submission strategies
● Provide planning, delivery communication of statistical analyses, data presentations, scientific reports, including clinical trial results, trial topline results, exploratory meta-analysis results
● Support fpublication activities, scientific presentations, 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, external regulatory, industry, professional academicganizations
● Accountable fstudy level submission level statistical deliverables on assigned projects
● Collaborate with project statisticians statistical leaders to establish consistent methodologies within the therapeutic area
● Ensure that all study project level statistical activities are conducted in compliance with the company processes relevant regulatory requirements
● Generate innovative ideas spearhead intricate projects across various business units
● Participate in research on statistical methodology its applications pertinent to business needs
● Engage in professional development activities both within outside theganization, ensuring continuous growth contribution to the field
Here Is What You Need (Minimum Requirements)
● PhD with at least 1 year of statistical consultation experience
● Proven track record in delivering timely high-quality statistical contributions scientific reports fclinical trials aimed at regulatory submissions
● Deep knowledge of experimental design cutting-edge technologies to enhance business processes
● Ability to identify, comprehend, apply pertinent scientific literature
● Strong written verbal communication skills fclear effective dissemination of information
● Experience in developing managing plans to achieve objectives
● Ability to operate independently in ambiguous situations make decisions to resolve moderately complex problems
Bonus Points If You Have (Preferred Requirements)
● Relevant pharmaceutical industry experience
● Expertise in biostatistical methodologies their application in clinical trials
● Experience with regulatory submissions interactions with health authorities
● Strong project management skills ability to lead complex projects
● Excellent collaboration teamwork skills
● Strong problem-solving skills ability to develop new options in non-standard situations
● Experience using common AI tools, including generative technologies such as ChatGPT Microsoft Copilot, to support problem solving enhance productivity. Demonstrated curiosity fexploring how these tools can improve outcomes understanding of responsible AI practices, including risk management ethical use
Work Location Assignment: On Premise
Pfizer is an equal opportunity employer complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on .
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