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Sr Manager, Biostatistics
Posted on May 1, 2025
- Oslo, Norway
- No Salary information.
- Full Time

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- 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
- 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
- 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 www.pfizer.no
- Please submit your application with CV and cover letter in English as soon as possible, no later than May 15th.
Work Location Assignment: Hybrid
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