Role Description
We are growing and seeking a Senior Research Scientist (Statistician) to join our Evidence Synthesis and Decision Modelling team. You will collaborate with a highly specialized team of statisticians, health economists, and researchers on global projects supporting evidence generation, comparative effectiveness research, health technology assessment (HTA), and decision-making for pharmaceutical and biotechnology clients.
Qualifications
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Master's degree or PhD in Statistics, Biostatistics, Epidemiology, Health Economics, Data Science, or a related quantitative discipline.
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Approximately 4 years or more of relevant professional experience.
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Strong R programming skills and experience conducting statistical analyses.
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Experience applying statistical methods to healthcare, outcomes research, evidence generation, or related research areas.
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Experience with evidence synthesis and comparative effectiveness research.
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Strong analytical reasoning and problem-solving skills.
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Ability to communicate complex findings clearly and effectively.
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Ability to work independently and as part of a multidisciplinary team.
Requirements
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Experienced Quantitative Researcher: Background in statistics, biostatistics, epidemiology, health economics, data science, or a related quantitative discipline.
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Evidence Synthesis and Statistical Methods Experience: Experience planning, conducting, and reporting analyses that support evidence synthesis and comparative effectiveness research.
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Technical Proficiency: Strong statistical programming skills, particularly in R, and experience developing reproducible analytical workflows.
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Deliverable Creation: Contribute to client-ready deliverables including analysis plans, technical reports, presentations, manuscripts, and conference materials.
Key Responsibilities
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Lead and deliver statistical analyses supporting evidence generation, comparative effectiveness research, and healthcare decision-making projects.
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Design and implement fit-for-purpose analytical approaches that address client objectives and research questions.
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Conduct statistical analyses and develop reproducible analytical workflows using R.
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Lead analytical workstreams and contribute to project planning, delivery, and quality assurance activities.
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Interpret and communicate complex analytical findings to technical and non-technical audiences.
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Support HTA, reimbursement, market access, and Joint Clinical Assessment evidence-generation activities.
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Mentor junior team members and contribute to methodological best practices.
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Contribute to scientific publications, conference presentations, proposals, and thought leadership activities.
Helpful Experience and Competencies
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Knowledge of indirect treatment comparison methodologies such as network meta-analysis (NMA), matching-adjusted indirect comparison (MAIC), simulated treatment comparison (STC), or similar approaches.
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Experience with external control arm (ECA) analyses.
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Experience with survival analysis, time-to-event modelling, or utility and health-related quality of life analyses.
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Experience working with individual patient level data.
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Understanding of Bayesian and/or frequentist statistical methods.
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Experience supporting HTA, reimbursement, market access, or evidence-generation activities.
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Familiarity with Python or other programming languages.
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Experience contributing to scientific publications or conference presentations.
Company Description