Career opportunities

This is a permanent position, on a full or part-time basis.



Your role:

• Applying innovative statistical approaches to solve novel data challenges
• Leading projects, ensuring efficient project management, compliance, and high-quality deliverables
• Leading and overseeing various statistical aspects of late-phase clinical trials in support of HTA submissions
• Reviewing of statistical analysis plans (SAPs) and quality controlling statistical output/reports
• Providing strategic statistical guidance to internal project teams and clients, ensuring scientifically sound and regulatory-compliant deliverables
• Engaging with clients to understand project requirements and ensuring client satisfaction
• Analysing and interpreting observational and real-world data
• Supporting systematic literature reviews, data extraction, and analysis
• Critically appraising the quality and reliability of data sources to support HTA decision-making
• Mentoring, training and providing expert guidance to junior colleagues
• Contributing to internal training initiatives, process improvement and business development

• MSc/PhD in Statistics/Biostatistics or equivalent knowledge/expertise with proven industry experience
• Solid understanding of the clinical drug development process
• Comprehensive knowledge of regulatory standards, ICH/GCP guidelines, and HTA regulations
• Proficiency in SAS
• Exceptional problem-solving abilities and attention to detail
• Ability to work independently and collaboratively in a team-oriented environment
• Fluent in written and spoken English

This is a permanent position, on a full or part-time basis.



Your role:

• Applying innovative statistical approaches to solve novel HTA-related data challenges
• Leading the analysis of patient data from clinical, observational, and real-world data trials in support of HTA submissions
• Developing / reviewing HTA-related analysis plans
• Producing / quality controlling statistical outputs, summaries, and reports
• Providing statistically related HTA guidance to internal project teams and clients
• Engaging with clients to understand project requirements and ensuring client satisfaction
• Supporting systematic literature reviews, data extraction, and analysis
• Conducting feasibility assessments of direct and indirect evidence
• Critically appraising the quality and reliability of data sources to support HTA decision-making
• Mentoring, training and providing guidance to junior colleagues
• Contributing to internal training initiatives, process improvement, and business development

• MSc/PhD in Statistics/Biostatistics or equivalent
• Solid understanding of the clinical drug development and HTA-related regulations and processes
• Familiarity with statistical methodology relating to direct/indirect evidence (NMA, ITC, MAIC)
• Proficiency in R and/or SAS
• Exceptional problem-solving abilities and attention to detail
• Ability to work independently and collaboratively in a team-oriented environment
• Fluent in written and spoken English