The Senior Principal Biostatistician is responsible and accountable for all statistical work, scientific and operational, for one or more assigned clinical trials in collaboration with the clinical trial team/global clinical team (GCT). You will work independently at the clinical trial level and may lead indication-level or project-level statistical activities for a drug development project under limited supervision. You will propose and lead implementation of modern and innovative trial/experimental designs, statistical models, analysis, and data exploration methodologies at the study or project level.

This role may be in Early Development, Full Development (Oncology, Immunology, Cardio-Renal Metabolic, or Neuroscience) Global Medical Affairs.

About the Role

Key requirements:

• Responsible for all statistical tasks on the assigned clinical trials and perform these tasks for mid- to high-complexity trials independently with peer review/input as required. Responsible for protocol development in alignment with the clinical development plan, developing statistical analysis plan, study and indication-level reporting activities.
• Contribute to planning and execution of exploratory analyses, PK, PK/PD analyses, exploratory biomarker and diagnostic analyses, and statistical consultation. Initiate, drive, and implement novel methods and innovative trial designs in alignment with the Lead Statistician.
• Explain statistical methodology and interpret analysis results. Provide statistical expertise to support submission activities and documents, significantly contributing to meetings with and responses to Health Authorities and other drug development activities, as required.
• Contribute to interactions with external review boards/ethics committees, external consultants, and other external parties with oversight as appropriate.
• Represent the Biostatistics & Pharmacometrics Line Function on cross-functional teams for the assigned trials. Responsible for functional alignment and ensuring line function awareness throughout the trials.
• Collaborate with other line functions. Explain statistical concepts in an easily understandable way to non-statisticians and provide adequate statistical justifications for actions/decisions/statements, when required.
• Establish and maintain collaborative relationships and effective communications cross-functionally within the Clinical Trial Team and Biostatistics & Pharmacometrics team.
• Ensure all Biostatistics deliverables for assigned clinical trials related activities are delivered in a timely manner with the highest level of quality.
• Propose and implement innovative designs and methods to optimize dose finding and drug development. Contribute to planning, prioritization, and tracking of program-level biostatistics activities and effective partnership with vendors.

Your Experience:

• MS (in Statistics or equivalent) with relevant work experience or PhD (in Statistics or equivalent) with relevant work experience.
• Fluent in English with strong communication and presentation skills.
• Influences decisions that directly impact the trial/project and team ability to deliver objectives.
• Demonstrable experience in all tasks of a statistician at trial level with the ability to work independently. Demonstrable knowledge and expertise in statistics and its application to clinical trials; ability to explain statistical designs and concepts. Depending on the assignment, it may require proven expertise in pharmacokinetics, exposure-response modelling, exploratory biomarker, diagnostic analyses, applied Bayesian statistics, or data exploration skills.
• Proficiency in the use of statistical software packages (e.g., SAS, R).
• Good knowledge of drug development and Health Authority guidelines.
• Demonstrated efficiency working on a multidisciplinary team to achieve team objectives.
• Understanding of Franchise/Therapeutic Area and/or regulatory activities.
• Good project management and matrix leadership skills. Ability to collaborate well with non-statistical functions.
• This role offers a hybrid working environment, requiring 3 days per week or 12 days per month in our London Office.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting, and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Commitment to Diversity & Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.