58 Statistician jobs in the United Kingdom

Statistical Scientist (Principal) – Hybrid / Remote, UK

A unique opportunity to contribute to innovative healthcare solutions as a Statistical Scientist This role supports the design, analysis, and reporting of clinical and observational studies, with a focus on patient-centric outcomes, often in rare or underserved disease areas.

You’ll collaborate across multidisciplinary teams and be involved in developing statistical methodologies, ensuring high-quality data interpretation, and delivering insights that guide critical decision-making in the development of new therapies.

What You’ll Do:

• Support planning and execution of clinical/observational studies, HTA, PK-PD, biomarker, or post hoc analyses
• Author and review protocols, SAPs, CRFs, TLF specs, and other key documentation
• Conduct statistical analyses in line with regulatory guidelines and best practices
• Collaborate with study team members across functions
• Develop expertise in therapeutic areas (particularly Oncology) and stay current with scientific and industry developments
• Contribute to clinical study reports and publications with clear statistical interpretation

What We’re Looking For:

• PhD with some experience, or a Master’s with significant experience in Biostatistics or a related field
• Strong R programming skills required; SAS knowledge a plus
• Experience in clinical trials, ideally in Oncology
• A collaborative mindset with a passion for applying statistical science in a real-world healthcare context

Working Environment:

This is a permanent hybrid role based in the UK , offering flexibility to work from home while maintaining meaningful in-person collaboration with colleagues.

We are committed to building a diverse and inclusive team.

Ready to make an impact in healthcare through innovative science and patient-focused solutions? Please get in touch with me

Principal Biostatistician | Global CRO | UK | Europe | Home-based

Global leading CRO have an opportunity for a Principal Biostatistician to join it’s expanding global team. This is a senior level opportunity where you will provide statistical leadership on the design, analysis, and interpretation of clinical trials, ensuring the highest standards of scientific and regulatory excellence.

What you will be doing:

• Serve as lead biostatistician across study programmes, regulatory submissions, and individual trials of varying complexity.
• Provide expert statistical guidance during interactions with clients and regulatory authorities.
• Review and approve statistical methodology within protocols, analysis plans, and clinical study reports.
• Develop and approve research proposals and budgets, delivering consultancy and statistical analyses for clients.
• Represent the organisation at bid defence meetings and contribute to business development presentations.
• Support projects across therapeutic areas including respiratory, vaccines, and oncology.

What you will need:

• Master’s degree or Ph.D. in Biostatistics, Statistics, or related discipline.
• Advanced expertise across statistical methodologies, therapeutic areas, clinical development, and programming practices.
• Proven ability to oversee and manage statistical activities across multiple programmes.
• Strong leadership skills with excellent communication, influencing, and project management experience.

What you will receive:

• Work for an award winning CRO that offers a supportive and flexible culture that values work-life balance and career development.
• Competitive salary with annual bonus, car allowance, and comprehensive benefits package including health insurance options, retirement planning and life assurance.
• Fully home based in the UK or across Europe.

What to do next:

If this opportunity aligns with your experience and career goals, please apply now with your CV.

Not the right fit?

For a confidential discussion about alternative opportunities, please contact Jo Fornaciari on

Principal Biostatistician – Leading CRO – Homebased – UK / Europe

We have recently partnered with an award winning CRO, who are looking for an experienced Principal Statistician, to join their successful study delivery team, any area of specialism considered

How you will be a success

The Principal Biostatistician will be accountable for the leadership of the Biostatistics and Programming activities of a program of studies of moderate complexity and/or of high value with high impact for the organization. Also responsible for planning, monitoring, organizing and reviewing activities of biostatisticians and programmers working on the assigned program of studies, ensuring individual studies and the overall program of studies and integrated analyses are delivered on time, on budget to required quality. Accountabilities also include maintenance of consistency across studies. Regulatory interaction experience also preferred.

Desirable Experience

• Biostatistical input into the design of the program, Protocol input such as study design, sample size calculations and patient randomization schemes and Statistical aspects of case report form design
• Review project database structures, edit checks and data management coding conventions
• Preparation of statistical analysis plans including the definition of derived data, and the design of statistical tables, figures, and data listings for clinical summary reports
• Statistical analysis, Interpretation of data and reporting of results
• Writing of the statistical methods sections of integrated study reports.
• Reviews draft integrated study reports.
• Supports responses to regulatory questions on the design of the program, and any labelling claims following submission
• Participates in presentations at client and investigator meetings
• Preparation of biostatistics input to company research proposals and participates in proposal defense meetings and makes presentations at marketing meetings with prospective client.

Key Qualifications and Skills

• M.S. or Ph.D. degree in statistics, biostatistics, or related field.
• Experience in statistics, biostatistics or related field
• Respiratory experience highly desired
• Accountable for leading Biostatistics and Programming activities for a program of studies of high complexity and/or of high value with high impact.
• Ongoing coaching and mentorship of team members.
• Knowledge of clinical trials methodology, regulatory requirements, statistics and statistical software packages, including SAS are a must.

What you get in return

Ongoing development is vital, and as a Principal Biostatistician you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. In comparison with their competitor’s and pharmaceutical companies, they provide more flexible working platforms for coaching and educating newcomers to be highly respected professionals in our industry.

They also provide successful candidates with an excellent employment package and benefits adapted to the current job market. The company like to look at themselves more like an extended family with consideration of staff as individuals allowing a work-life balance.

What to do next: If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome the new Statistician onboard as soon as possible.

Work from anywhere and shape powerful biostatistics that drive results! Enjoy the freedom of remote work while making a global impact.

Proclinical is seeking a Principal Biostatistician to lead programming activities for a program of studies. This role involves contributing to study design, statistical analysis, and regulatory submissions while ensuring consistency and quality across projects. You will work in a collaborative environment, mentoring team members and supporting client interactions.

Responsibilities:

• Lead biostatistics and programming activities for complex or high-value programs.
• Provide statistical input into study designs, including protocol development, sample size calculations, and randomization schemes.
• Review database structures, edit checks, and data management coding conventions.
• Develop statistical analysis plans, including defining derived data and designing tables, figures, and listings for clinical reports.
• Perform statistical analyses, interpret data, and report results.
• Write and review statistical methods sections of integrated study reports.
• Support responses to regulatory questions and contribute to labelling claims post-submission.
• Participate in client and investigator meetings, including presentations.
• Contribute to research proposals and participate in proposal defense meetings.
• Mentor and coach team members to foster professional growth.

Key Skills and Requirements:

• Advanced degree in statistics, biostatistics, or a related field.
• Strong understanding of statistical principles, experimental design, and regulatory requirements.
• Proficiency in statistical software packages, particularly SAS.
• Experience leading regulatory submissions.
• Excellent communication, interpersonal, and project management skills.
• Ability to translate client needs into statistical practices and educate stakeholders on statistical concepts.
  

If you are having difficulty in applying or if you have any questions, please contact Dean Fisher at

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -

Hobson Prior is seeking an Experienced Statistician to join a consultancy-based role in Manchester. This position offers the opportunity to work on diverse projects involving statistical analysis and evidence synthesis, with a focus on life sciences and evidence-based research. You will have the chance to take ownership of your work and grow your expertise in a supportive environment.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Lead projects involving statistical analysis, such as quality-of-life metrics, survival analysis, or evidence synthesis (e.g., meta-analyses, indirect comparisons).
• Use tools like R for data analysis and standard office software for documentation and communication.
• Take responsibility for your work from the start, with opportunities to develop and specialize based on your interests and strengths.

Key Skills and Requirements:

• Strong experience in applying and developing statistical methods in a professional setting, with a proven track record of delivering high-quality work.
• Backgrounds in consulting, academia, industry, or a mix of sectors are welcome, with particular relevance given to experience in life sciences or evidence-based research.
• A degree (2:1 or higher) in a quantitative field such as mathematics, economics, engineering, or a scientific discipline.
• Postgraduate qualifications (e.g., MSc or PhD) in statistics, health economics, or related areas are highly valued but not essential.

For more information, please contact Jack Gordon .

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -

Hobson Prior is seeking an Experienced Statistician to join a consultancy-based role in Manchester. This position offers the opportunity to work on diverse projects involving statistical analysis and evidence synthesis, with a focus on life sciences and evidence-based research. You will have the chance to take ownership of your work and grow your expertise in a supportive environment.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Lead projects involving statistical analysis, such as quality-of-life metrics, survival analysis, or evidence synthesis (e.g., meta-analyses, indirect comparisons).
• Use tools like R for data analysis and standard office software for documentation and communication.
• Take responsibility for your work from the start, with opportunities to develop and specialize based on your interests and strengths.

Key Skills and Requirements:

• Strong experience in applying and developing statistical methods in a professional setting, with a proven track record of delivering high-quality work.
• Backgrounds in consulting, academia, industry, or a mix of sectors are welcome, with particular relevance given to experience in life sciences or evidence-based research.
• A degree (2:1 or higher) in a quantitative field such as mathematics, economics, engineering, or a scientific discipline.
• Postgraduate qualifications (e.g., MSc or PhD) in statistics, health economics, or related areas are highly valued but not essential.

For more information, please contact Jack Gordon .

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - -policy.

We are seeking an experienced Principal Statistician to join our growing team. The successful applicant will work as part of global teams, supporting pharmaceutical, biotechnology and medical device companies across many therapeutic areas. Quanticate values quality first, integrity, care, people, commitment to delivery, and inspiration. As such, employees are offered flexible and friendly working conditions, competitive pay, industry-leading benefits, and opportunities for progression, in an environment where they are mixing with the very best experts in the field.

As Principal Statistician, you will be responsible for the development, validation, and implementation of statistical models and providing statistical support for clinical studies. You will serve as a Statistical Lead for large-scale clinical trials across various therapeutic areas, ensuring that all deliverables are achieved on time and to a high level of quality. You will lead Statistical Consultancy Projects, advising clients on all aspects of statistical trial design and conduct. Key to the role is, the ability to provide face to face advice to clients on all elements of study design, whether frequentist or Bayesian in nature. Having experience of using simulation methods in trial design would be an advantage but not essential. Through all activities you will also provide guidance and mentorship to other statisticians in the group.

Responsibilities

• Serve as lead statistician for clinical trials including planning, analysing, and reporting, ensuring that all deliverables are met on time and to a high level of quality.
• Develop and validate statistical models and analyses based on study protocols.
• Write statistical analysis plans and reports.
• Provide guidance and mentorship to other statisticians in the group.
• Collaborate with cross-functional teams to develop study protocols and ensure they meet regulatory requirements.
• To potentially take line management responsibility for junior statisticians within the team.
• To lead statistical consultancy projects as required, providing expert statistical advice on all statistical aspects of study design and conduct.
• Perform ad hoc statistical duties as required

Requirements

• Essential - MSc in Biostatistics, Medical Statistics or equivalent.
• Strong statistical expertise with experience in clinical trials.
• Experience in SAS programming.
• Extensive knowledge of regulatory requirements for clinical trials.
• Strong project management and leadership skills with experience leading large-scale projects.
• Excellent verbal and written communication skills.
• Ability to work independently and as part of a team.
• Willingness to travel when needed.

Benefits

• Competitive Salary (Open to discussion based on experience)
• Home working allowance
• Flexible working hours
• 25 days Annual leave plus bank holidays
• Option to purchase additional days holiday
• Pension with Company matching
• Private medical Scheme with Bupa
• Free standard eye test every two years
• Employee Assistance Program – Available for employee and immediate family
• 5, 10, 15 years of service recognition awards
• Death in service scheme
• Long Term Disability Insurance
• Quanticate offers a variety of different learning development opportunities to help you progress (mentoring, coaching, e-learning, job shadowing)

At Quanticate, we're pioneers in providing top-tier statistical and data management support to our clients. We're seeking a dedicated Statistician who's committed to upholding the highest standards, following procedures, and ensuring compliance with regulations, all while providing exceptional customer care.

As a Statistician your role will be playing a crucial role in supporting our clients and managing assigned project work. Here's what you'll be doing on a day to day basis:

• Handle statistical tasks, including producing tables, figures, and listings, and contributing to SAPs and statistical reports under the guidance of Senior and Principal Statisticians.
• Collaborate with Senior and Principal Project Delivery Managers, Portfolio Managers/Directors/VPs, and other team members to successfully deliver statistical activities.
• Organize and manage your workload, often working across multiple studies, ensuring work is completed on time and meets client expectations.
• Maintain effective communication with clients and internal stakeholders, providing regular updates on assigned work, addressing issues, and ensuring the delivery of high-quality, on-time, and budget-compliant outputs.
• Develop mentoring skills to advise other statisticians or programmers and contribute to knowledge-sharing activities.

We are dedicated to developing our staff and you will get regular opportunities to work autonomously, lead projects and mentor more junior staff to set you up for a Senior Statistician position in future.

Requirements

• Essential - An MSc in Medical Statistics or similar.
• Relevant experience as a statistician or biostatistician within the pharmaceutical industry or medical sector.
• Experience with clinical trials.
• Strong PC skills, including a working knowledge of Microsoft Office.
• Proficiency in SAS and other statistical software.
• Excellent written and oral communication skills.
• Strong organizational, analytical, and problem-solving skills.
• Effective interpersonal skills for working collaboratively with diverse teams.

Benefits

• Competitive Salary - Initial Banding of £31,000 - £38,000
• Flexible working hours
• 25 days Annual leave plus bank holidays
• Option to purchase additional days holiday
• Pension with Aviva – 5% from employee matched by Quanticate
• Private medical Scheme with Bupa
• Free standard eye test every two years
• Employee Assistance Program – Available for employee and immediate family
• 5, 10, 15 years of service recognition awards
• Death in service scheme
• Long Term Disability Insurance
• Quanticate offers a variety of different learning development opportunities to help you progress (mentoring, coaching, e-learning, job shadowing)

We are seeking an experienced Principal Statistician to join our growing team. The successful applicant will work as part of global teams, supporting pharmaceutical, biotechnology and medical device companies across many therapeutic areas. Quanticate values quality first, integrity, care, people, commitment to delivery, and inspiration. As such, employees are offered flexible and friendly working conditions, competitive pay, industry-leading benefits, and opportunities for progression, in an environment where they are mixing with the very best experts in the field.

As Principal Statistician, you will be responsible for the development, validation, and implementation of statistical models and providing statistical support for clinical studies. You will serve as a Statistical Lead for large-scale clinical trials across various therapeutic areas, ensuring that all deliverables are achieved on time and to a high level of quality. You will lead Statistical Consultancy Projects, advising clients on all aspects of statistical trial design and conduct. Key to the role is, the ability to provide face to face advice to clients on all elements of study design, whether frequentist or Bayesian in nature. Having experience of using simulation methods in trial design would be an advantage but not essential. Through all activities you will also provide guidance and mentorship to other statisticians in the group.

Responsibilities

• Serve as lead statistician for clinical trials including planning, analysing, and reporting, ensuring that all deliverables are met on time and to a high level of quality.
• Develop and validate statistical models and analyses based on study protocols.
• Write statistical analysis plans and reports.
• Provide guidance and mentorship to other statisticians in the group.
• Collaborate with cross-functional teams to develop study protocols and ensure they meet regulatory requirements.
• To potentially take line management responsibility for junior statisticians within the team.
• To lead statistical consultancy projects as required, providing expert statistical advice on all statistical aspects of study design and conduct.
• Perform ad hoc statistical duties as required

Requirements

• MSc in Biostatistics, Statistics or equivalent.
• Strong statistical expertise with experience in clinical trials.
• Experience in SAS programming.
• Extensive knowledge of regulatory requirements for clinical trials.
• Strong project management and leadership skills with experience leading large-scale projects.
• Excellent verbal and written communication skills.
• Ability to work independently and as part of a team.
• Willingness to travel when needed.

Benefits

• Competitive Salary (Open to discussion based on experience)
• Home working allowance
• Flexible working hours
• 25 days Annual leave plus bank holidays
• Option to purchase additional days holiday
• Pension with Company matching
• Private medical Scheme with Bupa
• Free standard eye test every two years
• Employee Assistance Program – Available for employee and immediate family
• 5, 10, 15 years of service recognition awards
• Death in service scheme
• Long Term Disability Insurance
• Quanticate offers a variety of different learning development opportunities to help you progress (mentoring, coaching, e-learning, job shadowing)