Director, Biostatistics

Position: Director, Real-World Biostatistics

Site Name: USA - Pennsylvania - Upper Providence, Durham Blackwell Street, UK – London – New Oxford Street, USA - Massachusetts - Waltham

Posted Date:
Dec 19 2025

The Director, Real-World Biostatistics is a key role focused on advancing strategy and methodology in the entire course of drug/vaccine development using real‑world data (RWD) within the enterprise. This position requires providing deep biostatistical expertise, strategic insight, and supporting methodological innovation to enhance the development and commercialization of pharmaceutical products, primarily in the oncology research unit (RU).

The Director will design and analyze RWD studies and other observational studies using cutting‑edge biostatistical methodologies associated with causal inference and comparative effectiveness, clinical outcomes assessment, longitudinal and predictive modelling, and target trial emulation, while also mentoring staff assigned to these projects.

Key Responsibilities Biostatistical and Methodologic Support

• Lead and oversee the execution of real‑world studies, ensuring methodological rigor, quality control, and regulatory adherence.
• Create and refine statistical analysis plans, conduct complex statistical analyses, and convey findings to internal and external stakeholders.
• Apply fit‑for‑purpose non‑interventional statistical methods tailored to specific study objectives, ensuring robust data interpretation and insight generation.

Therapy Area Knowledge

• Understand RU/assets to apply appropriate tools (e.g., variable definitions, code lists) and data sources and leverage hands‑on RWD expertise to guide the selection and appropriate use of complex health data sets, including experience authoring technical specification documents.
• Develop in‑depth knowledge on the assigned asset(s) and act as senior‑level RWB consultant on matrix teams.

Project Management and Staff Mentorship

• Mentor junior staff, guiding and developing their capabilities through mentorship, training, and professional growth opportunities while promoting knowledge sharing, continuous learning, and an innovative and collaborative environment.
• Lead statistical efforts for assigned projects, manage timelines, resources, quality control, and coordinate across departments (e.g., epidemiology, health economics and outcomes research, clinical).

Communication and Strategic Initiatives

• Engage in strategic communication within the organization and with external audiences presenting statistical analyses and insights clearly and effectively at conferences, in publications, and during key stakeholder meetings, reinforcing the value of biostatistical contributions.

Methodological Development and Innovation

• Stay informed on industry trends, incorporate emerging biostatistical methods to enhance study designs and analytics, and participate in methodological research for the development of analytical techniques.

Regulatory Support and Compliance

• Provide biostatistical expertise on RWD during regulatory submissions, meeting preparations, and addressing queries to ensure alignment with regulatory standards while offering statistical guidance for organizational decision‑making processes.
• Stay informed with guidance documents from regulators to industry on use of RWD for regulatory decision‑making.

Why you? Basic Qualifications

• Ph.D. in Biostatistics, Statistics, Epidemiology or related disciplines with 8+ years (or Masters plus 10+ years) of working within the pharmaceutical/biotech industry (preferably in real‑world evidence, epidemiology, or health outcomes functional areas).
• Experience working with drug development processes and strategies, utilizing innovative statistical skills to meet project and/or business objectives.
• Experience leading pharmacoepidemiology and/or health outcomes analytics using RWD (e.g., electronic health record; insurance claims; registries) and applying observational study design and biostatistical principles to clinical/epidemiological research.
• Experience in programming languages (e.g., R, Python) and applied experience with observational data.
• Experience in working according to regulatory requirements pertaining to RWD and clinical trials.
• Experience…