Senior/Principal Statistician
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Veramed
US
Summary
Provide high-quality statistical support and oversight for clinical studies and regulatory submissions for key FSP clients. Responsibilities include developing statistical analysis plans, performing sample size calculations, and potentially providing line management or project leadership.
Job Description
Veramed prides itself on two key areas: providing the highest quality statistical and programming consultancy to our clients, and offering our employees an industry‑leading working environment with outstanding support, training, and opportunities for career growth. We have an exciting opportunity for a Senior to Principal level Statistician to join us on a permanent basis. We offer flexible working (home, hybrid or office‑based), structured training and development, and a competitive package.
The Role
The purpose of this role is to provide high‑quality statistical support to one of our key FSP clients. As a Senior or Principal Statistician, you may also take on a supervisory role, including line management and/or project leadership, depending on experience and interest.This role is well‑suited to someone with significant experience in clinical studies and regulatory submissions, who is comfortable working directly with clients - including situations where there is no internal statistical support. You will be confident working independently, managing your own workload, and contributing across multiple projects and clients. Strong communication skills are essential, including the ability to explain statistical concepts to non‑statisticians and to present clearly and confidently to client teams.
Key Responsibilities
- Statistical oversight at study level
- Providing project‑level statistical input across clinical studies
- Review and oversight of statistical deliverables from other CROs
- Development and/or review of study documentation, including statistical sections of protocols and Statistical Analysis Plans (SAPs)
- Study design activities, including sample size calculations, ad‑hoc and exploratory analyses
- Additional statistical support as required across client projects
- Confident coding in R, SAS, or other non‑SAS languages (or a willingness to learn)
Experience & Skills
Essential:
- Senior to Principal level 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 the ability to explain statistical concepts to non‑statisticians
- Curious, proactive, and motivated to continuously learn and improve
Desirable:
- Study design and sample size experience
- Regulatory experience
- A basic understanding or willingness to learn Bayesian methods and causal inference modelling
- Experience within Oncology and/or CNS therapeutic areas
Opportunities at Veramed
- 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
What to Expect
- A warm, friendly working environment where you can thrive both personally and professionally
- Supportive, open‑door management that actively encourages development
- Exposure to a wide variety of clients and projects, including collaboration with leading global pharmaceutical companies
- The opportunity to work with a truly unique CRO that does things differently — valuing people, relationships, and quality
- The chance to genuinely own your role and shape your career path
If you’re independent, curious, and ready to make a meaningful impact within a forward‑thinking organisation, we’d love to hear from you.
Veramed is a B Corp accredited company which means that we use the power of business to build a more inclusive and sustainable economy meeting the highest verified standards of social and environmental performance, transparency, and accountability.
As an organisation that has people at the heart of it, Veramed is committed to creating a diverse environment and is proud to be an equal opportunities employer. We foster a working culture where employees have integrity, honesty and respect for one another without regard to race, national origin, religion, gender identity or expression, sexual orientation or disability. All qualified applicants will receive equal consideration for employment.
Veramed is a Clinical Research Organization (CRO) that provides expert data management, biostatistics and programming services to the pharmaceutical and biotech industry. With precision, consistency and an unwavering commitment to quality, Veramed is dedicated to setting the highest standards for biometrics in clinical trials.
Founded in 2012, Veramed has always been guided by quality, integrity and humanity. This means a culture that genuinely cares for its employees, and employees that genuinely care about the work they do, enabling unparalleled collaboration for industry-leading delivery.
Veramed’s growing team of expert data managers, statisticians and statistical programmers supports analysis and consultancy of Phase I-IV clinical trials across a variety of therapeutic areas. Whether it’s long-term partnerships or rapid-fire project work, Veramed works as an extension of clients’ teams, driving efficient, dependable outcomes.
A truly global CRO, Veramed is headquartered in Twickenham, England, with offices across the UK, Europe, US and India. Veramed is proud to be B Corp Certified ®, committed to integrity and impact in everything we do.
Our vision
We exist to set the new standard for biometrics. By making the right decisions – for our employees, for sponsors, and for patients – we’re redefining what biometrics can deliver in clinical trials.
Founded
2012
Company size
501-1,000 employees
Industry
Research Services
Org type
Privately Held
Headquarters
London
Veramed is a Clinical Research Organization (CRO) that provides expert data management, biostatistics and programming services to the pharmaceutical and biotech industry. With precision, consistency and an unwavering commitment to quality, Veramed is dedicated to setting the highest standards for biometrics in clinical trials.
Founded in 2012, Veramed has always been guided by quality, integrity and humanity. This means a culture that genuinely cares for its employees, and employees that genuinely care about the work they do, enabling unparalleled collaboration for industry-leading delivery.
Veramed’s growing team of expert data managers, statisticians and statistical programmers supports analysis and consultancy of Phase I-IV clinical trials across a variety of therapeutic areas. Whether it’s long-term partnerships or rapid-fire project work, Veramed works as an extension of clients’ teams, driving efficient, dependable outcomes.
A truly global CRO, Veramed is headquartered in Twickenham, England, with offices across the UK, Europe, US and India. Veramed is proud to be B Corp Certified ®, committed to integrity and impact in everything we do.
Our vision
We exist to set the new standard for biometrics. By making the right decisions – for our employees, for sponsors, and for patients – we’re redefining what biometrics can deliver in clinical trials.
Founded
2012
Company size
501-1,000 employees
Industry
Research Services
Org type
Privately Held
Headquarters
London