Use Your Power for Purpose
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. By investigating ways to close data gaps and developing frameworks, you will contribute to the safe and appropriate use of medicines for patients, making a significant impact on global health.
What You Will Achieve
In this role, you will:
Design, plan, and execute biostatistical components for research and development projects
Develop and lead/co-lead complex projects, managing plans to achieve objectives
Make decisions to resolve moderately complex problems, developing new options guided by policies in non-standard situations
Operate independently in ambiguous situations, using knowledge and experience to achieve desired results
Work indirectly reviewed through consultation and agreement and may review work of others in Sub Business Unit
Generate innovative ideas and spearhead intricate projects across various business units
Collaborate with project statisticians and statistical leaders to establish uniform global systems and processes
Facilitate the planning, execution, and dissemination of statistical analyses, data presentations, and scientific reports, including clinical trial outcomes and support for publication endeavors
Engage in professional development activities both within and outside the organization, ensuring continuous growth and contribution to the field
Here Is What You Need (Minimum Requirements)
BA/BS with at least 6 years of experience or MBA/MS with at least 5 years of experience or PhD/JD with at least 1 year of experience or MD/DVM with any years of 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
Bonus Points If You Have (Preferred Requirements)
Master's degree with relevant pharmaceutical industry experience
Expertise in biostatistical methodologies and their application in clinical trials
Experience with regulatory submissions and interactions with health authorities
Strong project management skills and ability to lead complex projects
Excellent collaboration and teamwork skills
Strong problem-solving skills and ability to develop new options in non-standard situations
Further information
This position is located in Lysaker, Oslo, Norway on permanent contract. Role is flexible with an average of 2,5 days/week in the office.
To find out more about Pfizer Norway, visit us and learn more at
Please submit your application with CV and cover letter in English as soon as possible, no later than May 15th.
Work Location Assignment: Hybrid
Equal Employment Opportunity
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.
Disability Inclusion
Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
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