Similar Jobs at Pfizer
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
The Manager, Global Labeling Lead is responsible for leading the global labeling strategy, managing the labeling process, and collaborating with cross-functional teams in the pharmaceutical industry.
Top Skills:
Core Data SheetsEu Summary Of Product CharacteristicsUs Prescribing Information
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:
Here Is What You Need (Minimum Requirements)
Bonus Points If You Have (Preferred Requirements)
Further information
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!
Medical
#LI-PFE
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 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
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!
Medical
#LI-PFE
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