Principal Statistician – Remote, United Kingdom
Department: Statistics / Clinical Programming
Employment Type: Full-Time | Remote
Experience Required: 8+ years in clinical statistics or related roles
Job Summary
Quanticate, a global, data-focused Contract Research Organization (CRO), is seeking an experienced Principal Statistician to join our UK-based remote team. This role offers the opportunity to lead statistical activities across pharmaceutical, biotechnology, and medical device clinical trials, contributing to high-quality decision-making and ensuring regulatory compliance.
The ideal candidate will combine technical expertise, strategic thinking, and leadership skills, serving as a statistical lead for complex clinical trials across multiple therapeutic areas. Quanticate fosters a culture of quality, integrity, and collaboration, providing flexible working conditions, competitive compensation, and opportunities for career progression.
Key Responsibilities
Lead statistical activities for clinical trials, including planning, analysis, and reporting, ensuring timely and accurate deliverables.
Develop, validate, and implement statistical models in alignment with study protocols.
Prepare statistical analysis plans (SAPs) and reports.
Provide mentorship and guidance to junior statisticians and project teams.
Collaborate with cross-functional teams to ensure study protocols meet regulatory standards.
Lead statistical consultancy projects, offering expert advice on trial design, frequentist and Bayesian approaches, and analysis strategies.
Utilize simulation methods for trial design where applicable.
Perform ad hoc statistical duties as required by projects or clients.
Required Qualifications & Skills
MSc or equivalent in Biostatistics, Medical Statistics, or related quantitative field.
8+ years of hands-on experience in clinical statistics within pharma, biotech, or CRO settings.
Expertise in adaptive trial designs, Bayesian statistics, and SAS programming.
Strong knowledge of regulatory requirements for clinical trials (ICH/GCP, EMA, FDA).
Proven project management and leadership capabilities, including experience managing large-scale clinical projects.
Excellent written and verbal communication skills for client interactions and cross-functional collaboration.
Ability to work independently in a remote environment while supporting global teams.
Willingness to travel occasionally for client meetings or training.
Why Join Quanticate?
Work remotely on global clinical trial programs in a collaborative, flexible environment.
Lead complex and impactful statistical projects across multiple therapeutic areas.
Contribute to the development of cutting-edge clinical therapies.
Engage with a culture that prioritizes quality, integrity, and continuous learning.
Opportunities for professional development through mentoring, coaching, e-learning, and professional society memberships.
Benefits
Competitive salary (open to discussion based on experience)
Flexible working hours and home working allowance
25 days annual leave plus UK bank holidays; option to purchase additional leave
Company-matched pension scheme
Private medical insurance (Bupa) for self and immediate family
Employee Assistance Program (EAP) for employee and family
Free standard eye test every two years
Long-term disability insurance and death-in-service benefits
Service recognition awards at 5, 10, and 15 years
Gujarat :
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Andover | Billerica | Boston | Cambridge | Devens | Lexington | Massachusetts | Medford and Somerville | Rockland |Wisconsin :
Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Arkansas | Remote Australia |New South Wales :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Paris | Lyon |South Africa :
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