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Provide expert input on the design of clinical development programs to ensure Access/HTA evidence needs are considered within global development and commercialization strategies
Identify evidence gaps, possible data sources, and design and implement robust evidence-generation plans
Ensure Access/HTA evidentiary activities are strategically aligned with other functions within Global Access and the wider organization (affiliates, Product Development, commercial, etc.)
Plan and conduct statistical analyses of clinical trials and other relevant data sources and develop supporting technical documentation for statistical analyses and economic models
Interpret and communicate the findings of analyses and work closely with affiliates to incorporate global statistical and health economics input into their local reimbursement applications
Lead or contribute to cross-functional teams within a matrix structure and actively contribute to the development of methodologies and continuous improvement within the Evidence Chapter
Keep up to date with the changing Access/HTA landscape and academic research to ensure current access trends and methodologies are incorporated into evidentiary plans and build relationships with relevant external statistics, health economics, Access/HTA, and policy experts
Ensuring that all assigned projects are being conducted in an efficient manner and that quality and client satisfaction is maximized at all times
Guide the Senior associates and Associates in their daily duties and to flag any areas of acute training needs to their line managers
Maintaining client relationships on their projects
Independently contributing to the preparation of network meta-analysis protocols, reviewing data extracted from systematic literature reviews, conducting feasibility assessments, generation of network diagrams, critical assessment of study heterogeneity, conducting network meta-analysis, and assisting with the interpretation and dissemination of findings
Requirements
A Master's or Doctoral-level degree in applied statistics, health economics, and related quantitative fields
A minimum of 3 years of hands-on experience working in the pharmaceutical industry, a consultancy, Access/HTA/reimbursement agency, or academic institution (pharma affiliate experience is a plus)
Demonstrate in-depth knowledge of Access and HTA, clinical research and development methods, and international payer evidence requirements
Skilled in research design and statistical methods, such as Generalized Linear Models, Survival analysis, Network Meta-Analysis, and Bayesian statistics and are proficient in R and GitLab (experience with SAS, Python, WinBUGS, JAGS, or other relevant statistical software is a plus)
Strong strategic, collaboration, and communication skills, strong organization, planning, and prioritization skills with an ability to meet tight deadlines, and strong written and verbal communication skills in English
Nice to have
experience with SAS, Python, WinBUGS, JAGS, or other relevant statistical software