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About the Role
The Manager, Statistics provides statistical expertise to support the research and development organization, working independently in partnership with experts in multiple disciplines to advance medicines to our patients.
Responsibilities
- Provide expertise to design, analysis and reporting of clinical trials or other scientific research studies.
- Independently develop protocols and/or statistical analysis plans with details for programming implementation.
- Implement sound statistical methodology in scientific investigations.
- Identify scientifically appropriate data collection instruments.
- Identify and report data issues or violations of study assumptions.
- Provide programming specifications for derived variables and analysis datasets.
- Partner with Data Science in preparing for database lock.
- Independently perform statistical analyses as per the analysis plan.
- Collaborate with Statistical Programming to ensure the delivery of high-quality outputs according to agreed-upon timelines.
- Identify and anticipate issues arising in the study design, conduct and propose scientifically sound approaches.
- Evaluate appropriateness of available software for planned analyses and assess needs for potential development of novel statistical methodology.
- Develop strategy for data presentation and inference.
- Collaborate in publication of scientific research.
- Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures.
- Ensure that study results and conclusions are scientifically sound, clearly presented, and consistent with statistical analyses provided.
- Work collaboratively with multifunction teams.
- Clearly explain statistical concepts to non-statisticians.
- Provide responses to questions, and pursue analyses suggested by data.
- Support communications between assigned product team(s) and functional management.
- Build/drive cross-functional relationships and collaboration.
Requirements
- MS (with 6+ years of experience) or PhD (with 2+ years of experience) in Statistics, Biostatistics, or a highly related field.
- Experience performing statistical computations and simulations
- Clinical Trial experience
- Pharmaceutical or CRO experience
- Oncology research trial experience
- Experience applying AI to statistical work
- Understanding of drug development and life-cycle management in the regulated environment.
- High degree of technical competence and effective communication skills, both oral and written
- Able to identify data or analytical issues, and assist with providing solutions by either applying own skills and knowledge or seeking help from others
- Able to build strong relationship with peers and cross-functional partners to achieve higher performance.
- Highly motivated to drive innovation by raising the bar and challenging the status quo
Skills
- Statistics
- Biostatistics
- Statistical computations
- Simulations
- Clinical Trial design
- Clinical Trial analysis
- Clinical Trial reporting
- Protocol development
- Statistical analysis plans
- Product safety analysis plans
- Integrated summary of safety analysis plans
- GMA evidence generation analysis plans
- Data collection instruments
- Data issue identification
- Study assumption violation reporting
- Programming specifications
- Derived variables
- Analysis datasets
- Database lock preparation
- Statistical analysis
- Statistical programming
- Study design
- Study conduct
- Statistical methodology
- Software evaluation
- Novel statistical methodology development
- Data presentation strategy
- Inference strategy
- Scientific publication
- Report accuracy
- Report internal consistency
- Publication accuracy
- Publication internal consistency
- Table generation
- Listing generation
- Figure generation
- Study results interpretation
- Study conclusions interpretation
- Multifunction team collaboration
- Statistical concept explanation
- Communication
- Problem-solving
- Relationship building
- Cross-functional collaboration
- Innovation
- Challenging the status quo
Experience Level
- 6+ years of experience (MS)
- 2+ years of experience (PhD)
Education Level
- MS in Statistics, Biostatistics, or a highly related field
- PhD in Statistics, Biostatistics, or a highly related field
Salary/Compensations
- USD 109500 - USD 208500 - yearly
Benefits
- Paid time off (vacation, holidays, sick)
- Medical/dental/vision insurance
- 401(k)
- Long-term incentive programs
About the Company
- AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow.
- We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio.
- For more information about AbbVie, please visit us at www.abbvie.com.
- Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Equal Opportunity
- AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.
- Equal Opportunity Employer/Veterans/Disabled.
- US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
- US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html