Posted 6d ago

Senior Director, Biostatistics

@ Orchard Therapeutics
London, England, United Kingdom
HybridFull Time
Responsibilities:lead statistics, direct development, regulatory liaison
Requirements Summary:15+ years as a statistician in drug development, 5+ years in management; MSc or PhD; strategic input; strong communication; SAS; CDISC; regulatory submission lead.
Technical Tools Mentioned:SAS, R, CDISC
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Job Description

Location: London/Hybrid

 

Orchard Therapeutics, a Kyowa Kirin company, is a global gene therapy leader focused on transforming the lives of patients with rare disorders through innovative gene therapies based on gene-modified hematopoietic stem cells (HSCs). Orchard has its global headquarters in London, England.

Job Summary

The Senior Director, Biostatistics is the head of Orchard’s Biostatistics function and a key member of the Medical/Clinical Development team, working to provide transformative gene therapies to patients.  This role provides a unique opportunity to contribute strategic statistical thinking to clinical drug development across multiple programs, in a dynamic environment. You will be the primary voice for statistical innovation, ensuring that our gene therapy candidates are evaluated using the most robust and efficient methodologies available. This role requires a blend of deep technical expertise and the presence to interact effectively with both internal stakeholders and global regulatory agencies.

The position will report to the VP, Clinical Science and will have management responsibility for a team of statisticians and programmers.

 

Key Responsibilities

·         Team building: Build and lead a high-performing Biostatistics team, promote collaboration and advance professional development. Develop and monitor departmental objectives. Ensure adherence to annual budget targets, including effective oversight of third-party vendors.

·         Strategic leadership: Provide input into clinical development plans to ensure statistical integrity, compliance with regulatory requirements, and alignment with Orchard’s objectives.

·         Cross-functional and external collaboration: Partner with clinical, regulatory, and medical affairs colleagues, and with external partners and vendors, to support the clinical development of Orchard’s assets.

·         Innovation: Explore and implement novel statistical methodologies where possible, considering specific requirements for gene therapy (one time administration and long-term follow-up) and rare disease/small populations.

·         Regulatory engagement: Represent Orchard as the lead statistician during interactions with global regulatory and health technology agencies. Review/contribute to regulatory briefing documents, defend the statistical integrity of regulatory submissions, and respond to technical questions from agencies.

·         Study design and execution: Provide statistical input as required, including sample size justification, specification of estimands, oversight of SAP/shell production, oversight of vendors, and ensuring correct interpretation of results in study reports and submission documents.