Career opportunities

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

Your role:

• Converting clinical research questions into statistical/epidemiological modelling concepts
• Synthesising, analysing and interpreting clinical trial data using SAS and/or R
• Providing statistical consulting as an active member of a project team

• BSc/MSc in Statistics/Biostatistics or equivalent knowledge/expertise
• Graduates and career-young (Bio)statisticians (1 – 2 years experience) are encouraged to apply
• Team player with strong communication skills
• Knowledge in statistical programming languages preferred (SAS and/or R), with the willingness to become proficient in SAS programming
• Fluent in written and spoken English
• Legal right to live and work in the UK

• A supportive, experienced team, an excellent atmosphere with an open-door policy
• A workspace in our office in Wokingham with the possibility of hybrid working
• Flexible working conditions and continuous training
• A varied range of tasks with development opportunities

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