Veramed
Senior or Principal Statistician - UK/EU (Remote/ Hybrid/ Office)
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Clinical Trials Statistician – Senior/Principal
Clinical trials are high stakes, demanding high standards. Veramed sets this standard by bringing together the sharpest minds in data management, biostatistics, and programming, backed by cutting-edge technology and proven processes.
Our globally connected, caring team delivers quality, precision, and collaboration, earning trust through consistency and integrity. From rapid-fire project work to long-term partnerships, Veramed brings the right minds to every challenge.
About the Role
The purpose of this role is to provide high-quality statistical support and take on responsibilities aligned with experience and interest, including:
- Supervisory roles (e.g., line management, project leadership)
- Direct client engagement, particularly in scenarios with no internal statistical support
- Independent project management with a focus on delivering excellence
Ideal candidates bring significant experience in clinical studies and regulatory submissions, are comfortable working without immediate supervision, and understand client-facing demands. Strong communication skills are essential—including translating statistical concepts for non-specialists and delivering presentations to client teams confidently.
Key Responsibilities
- Statistical oversight of clinical studies at project level
- Provision of statistical input across the lifecycle of clinical studies
- Review and oversight of statistical deliverables from other Contract Research Organizations (CROs)
- Development and/or review of study documentation, including:
- Statistical sections of protocols
- Statistical Analysis Plans (SAPs)
- Study design activities, such as:
- Sample size calculations
- Ad-hoc and exploratory analyses
- Additional statistical support across client projects as required
- Confident coding in R, SAS, or other non-SAS languages (or readiness to upskill)
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Experience & Skills
Essential Qualifications & Skills
- Senior to Principal-level experience as a statistician in a clinical research environment
- Hands-on experience in:
- Clinical studies execution
- Regulatory submissions
- Ability to work independently with client-facing accountability
- Strong communication skills—ability to:
- Simplify complex statistical concepts
- Present findings effectively to non-technical teams
- Curiosity, initiative, and a drive for continuous learning
Desirable Experience & Skills
- Study design and sample size calculation expertise
- Regulatory submissions experience
- Basic knowledge or willingness to learn (self-direct) in:
- Bayesian methods
- Causal inference modelling
- Specialisation in Oncology and/or CNS (Central Nervous System) therapeutic areas
Opportunities at Veramed
- Publication & career growth:
- Authorship of conference papers and peer-reviewed publications
- Innovative methodologies:
- Develop and implement progressive statistical techniques, study designs, and efficiency optimisations
- Leadership & mentorship:
- Line management and peer guidance opportunities
- Contribution to business process improvement
- Internal training on statistical best practices
- Ethical & social impact:
- Support employee welfare, environmental initiatives, and community engagement as part of Veramed’s B Corp accreditation
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What to Expect
At Veramed, you’ll experience:
✅ A collaborative, people-first culture where personal and professional growth are prioritised ✅ Supportive, transparent leadership with open-door policies and development mentorship ✅ Diverse project exposure, collaborating with global pharmaceutical leaders and multinationals ✅ A unique CRO model that values integrity, relationships, and high-quality outputs—unlike traditional industry approaches ✅ Ownership and career shaping responsibility—you can drive your role’s direction based on interests and strengths
If you’re independent, curious, and eager to make an impact in a forward-thinking, Values-Driven organisation, we’d love to hear from you!
Veramed's Commitment
Veramed is a B Corp-accredited company, leveraging business for good to build a more inclusive, sustainable future. We meet the highest social, environmental, and transparency standards.
We promote an inclusive workplace and are an equal opportunities employer, valuing diversity in all forms (race, origin, religion, gender identity, sexual orientation, disability). Every qualified applicant receives equitable consideration.
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