Senior Statistician, Research

Position Summary

We are seeking a motivated and technically strong statistician to join our DSS team in China. In this role, you will support statistical planning, analysis, and China regulatory interaction/submissions for clinical trials conducted in China and globally. This position is ideal for recent graduates or individuals transitioning into the pharmaceutical industry, who are eager to learn and contribute to meaningful healthcare innovations. You will work under the guidance of experienced statisticians and cross-functional teams to develop hands-on skills in drug development.

Major Job Responsibilities

• With supervision, assist in the development of clinical trial protocols and statistical analysis plans (SAPs) with details for programming implementation.
• Support study design elements such as sample size estimation, randomization strategy, and endpoint definitions
• Assist in identifying scientifically appropriate data collection instruments or fit-for-purpose data sources. With supervision provide programming specifications for derived variables and analysis datasets. Assist Data Science in preparing for database lock
• With supervision 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.
• With supervision, provide appropriate interpretation of statistical deliverables in collaboration with other functions. Collaborate in publication of scientific research. Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures.
• Collaborate effectively with both Global and China-based teams, acting as a communication bridge to align statistical deliverables and ensure mutual understanding of clinical and regulatory expectations.
• Participate in local regulatory deliverables including statistical review documentation
• Explore and apply AI-powered tools to solve business problems, increase productivity and improve effectiveness under supervision.

Qualifications

Qualifications

• MS (with 4+ years of experience) or Ph. D degree in Statistics, Biostatistics, Applied Mathematics, or a related field
• Familiarity with at least one statistical programming language (e.g., SAS, R, Python)
• Solid foundation in statistical concepts and basic clinical trial design principles
• Able to perform statistical computations and simulations
• 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.
• Excellent written and verbal communication skills in both Mandarin and English.
• A proactive learner with strong ability to work in a team-based environment.

Preferred Qualifications

• Internship or academic project experience related to clinical data, healthcare analytics, or predictive modeling
• Understanding of CDISC standards or regulatory framework (eg, ICH guideline)
• Exposure to AI-based tools or programming libraries

Key Stakeholder:

• Clinical development experts
• Statistical programmers
• Data science experts
• Regulatory affair experts

Additional Information

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