Location: UK (hybrid in our London offices or remote working) or Ireland

Duration: Permanent

Start date: flexible between September 2026 to latest February 2027

Important information:

• Applications are open until June 7th
• We can only accept applicants who are based in UK/ Ireland, or who are eligible to work in UK/Ireland.
• Please submit a cover letter that includes your motivation for the program and from when you would be available to start. Thank you.

Major accountabilities:

• All statistical tasks on assigned trials, where you will be expected to perform these tasks independently, seeking peer input/review as required. Tasks may include: protocol and statistical analysis plan development; reporting activities; contributing to the planning and execution of exploratory analyses and/or PK, PK/PD analyses; exploratory biomarker and diagnostic analyses; statistical consultation. You will be responsible for initiating, driving and implementing novel methods and innovative trial designs in alignment with the Lead Statistician.
• Explaining statistical methodologies and interpreting analysis results. You will provide statistical expertise to support submission activities and documents, meetings with and responses to Health Authorities and other drug development activities.
• Contributing to interactions with external review boards, ethics committees, external consultants, and other external parties with oversight. You may represent Novartis in statistical discussions at external congresses, conferences or scientific meetings.
• Representing the AQS line function in multi-functional teams for the assigned trials. You will have responsibility for ensuring functional alignment and line function awareness of the status and issues related to the assigned trials.
• Collaborating with other line functions. You will explain statistical concepts in a manner that is easily understood by non-statisticians and provide adequate statistical justifications for actions/decisions/statements.
• Establishing and maintaining sound working relationships and effective communication with the Clinical Trial Team and quantitative sciences team.
• Overseeing all Biostatistics resources and work for assigned trials and/or related non-clinical activities, and ensuring work is timely and of adequate quality.

Essential Requirements:

• PhD (in Statistics, Mathematics, Computational Sciences, Data Science, or equivalent); PhD needs to be completed before your start date; Candidates may have up to 2 years of post-PHD experience, provided it has been gained in academia; prior industry experience in similar roles will not be considered.
• Proven knowledge and expertise in statistics and its application to clinical trials or public health
• Proficiency in statistical software packages (e.g. R)
• Ability to influence decisions that directly impact the assigned clinical trial and team ability to deliver objectives
• Good communication and presentation skills, ability to work on and collaborate seamlessly with a multidisciplinary team to achieve team objectives
• Proficiency in English (oral & written)

Desirable:

• Depending on your assignment, you it may be helpful to have expertise in one or more of the following areas: Bayesian statistics, causal inference, clinical trial design, data exploration skills, estimands, evidence synthesis, pharmacokinetics, machine learning, missing data, modelling approaches.

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

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
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