Statistical Programming Lead

Statistical Programmer

We are recruiting for multiple Statistical Programmers. As part of a cross‑functional global team, this role independently drives programming activities across clinical and Medical Affairs studies — including exploratory, PK/PD, biomarker, and regional projects. You’ll take ownership of all programming deliverables at both study and submission levels within assigned focus areas, ensuring accuracy, consistency, and compliance.

You'll lead as a Global Programmer (GPROGL) for early‑stage or non‑complex assets, oversee programming vendors, and support data transparency by preparing regulatory disclosure summaries. The role also contributes to departmental initiatives and, under guidance, may develop complex TLFs, lead late‑phase programs, or mentor other programmers.

• Developing and executing high‑quality, on‑time statistical analysis and reporting deliverables (e.g., SDTM/ADaM datasets, tables, listings, figures).
• Collaborating closely with statisticians, ensuring specifications are complete and statistical plans are executed efficiently with the right level of validation.
• Acting as the single point of contact for assigned studies, coordinating the activities of the programming team internally, and liaising with vendor lead programmers when needed.
• Enforcing Astellas, industry, and regulatory standards across all programmed deliverables (including CDISC datasets and internal TLF standards), ensuring submission‑ready outputs.
• Participating in developing and implementing programming tools that strengthen Statistical Programming infrastructure projects.
• Leading programming activities related to clinical trial data disclosure for regulatory and research‑based submissions.
• Communicating efficiently and regularly with the Global Programmer Lead (GPROGL) and/or line management on study, project, and resource status.

• Solid experience in statistical programming within the pharmaceutical industry, including experience working with external vendors.
• Proven track record leading programming activities for drug development programs.

• Bachelor’s or master’s in statistics, mathematics, or related field or equivalent.

• The is a permanent full‑time position based in the UK.
• This position follows our hybrid working model. Role requires a blend of home and a minimum of 1 day per quarter in our Addlestone office. Flexibility may be required in line with business need. Candidates must be located within a commutable distance of the office.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.