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Senior, Principal Statistician

🔥 40 minutes ago

🌐 United Kingdom, Poland – Remote

infoinfo

⏰ Full Time

🟠 Senior

Where this job comes from

Posted on Veramed's careers page, not through a job board

First seen by Remote Rocketship 40 minutes ago

Still open on Veramed's site. Checked 22 minutes ago.

Logo of Veramed

Veramed

501 - 1000 employees

Founded 2012

🏥 Healthcare

💊 Pharmaceuticals

🧬 Biotechnology

Healthcare • Pharmaceuticals • Biotechnology

Veramed is a biometrics-focused contract research organization (CRO) that provides data management, biostatistics, programming, evidence & value generation, and standards/AI services to pharmaceutical and biotechnology clients. The company offers end-to-end biometrics support, Functional Service Provider (FSP) and project-based delivery models, regulatory submission-ready data, advanced automation and AI (Veramed. ai), CDISC compliance, and data visualization to minimize submission issues and audit findings. Veramed positions itself as a trusted partner for biotech and pharma, emphasizing operational governance, scalability, and a people-first culture.

📋 Description

• Provide high-quality statistical support • Take on supervisory responsibilities, including line management and/or project leadership, depending on experience and interest • Provide statistical oversight at study level • Provide project-level statistical input across clinical studies • Review and oversee statistical deliverables from other CROs • Develop and/or review study documentation, including statistical sections of protocols and Statistical Analysis Plans (SAPs) • Conduct study design activities, including sample size calculations, ad-hoc and exploratory analyses • Provide additional statistical support across client projects • Work across multiple projects and clients • Explain statistical concepts to non-statisticians and present clearly to client teams

🎯 Requirements

• Senior level (4+ years) experience in statistics within a clinical research environment • Experience working on clinical studies and regulatory submissions • Comfortable working independently with clients, often without in-house statistical support • Strong communication skills and ability to explain statistical concepts to non-statisticians • Curious, proactive, and motivated to continuously learn and improve • Confident coding in R, SAS, or other non-SAS languages, or willingness to learn

🏖️ Benefits

• Office based, hybrid and remote opportunities • Presenting at conferences and authoring publications • Developing and implementing innovative statistical methodologies, study designs, and efficiency-optimisation ideas • Line management and peer mentoring opportunities • Contributing to business process improvements and internal training • Supporting initiatives linked to employees, the environment, and local communities as part of our B Corp accreditation • Warm, friendly working environment • Supportive, open-door management that actively encourages development • Exposure to a wide variety of clients and projects, including collaboration with leading global pharmaceutical companies • Opportunity to work with a unique CRO valuing people, relationships, and quality • Opportunity to own the role and shape career path • Equal opportunities employer and diverse working environment

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