Overview
HTA Evidence Synthesis Statistician role at Novartis Ireland. Lead the design and execution of evidence-synthesis for HTA submissions (EU HTA JCA Dossier) and health economic models. Apply methodological and analytical expertise to demonstrate the value of Novartis assets and tailor evidence for external decision makers. This role supports the International HEOR & PCO Team within International Value & Access.
Key Responsibilities
* Develop core global Indirect Treatment Comparison (ITC) plans for HTA, payer and other Access stakeholder assessments, submissions, and negotiations. Lead publications associated with these efforts.
* Provide strategic, methodological, and analytical support to regions and key countries; adapt ITC for local HTA submissions and support local HTA strategy. Coordinate data requirements across evidence generation functions to support Pricing & Reimbursement.
* Set up systems to capture HTA analytic requirements across international markets; inform and optimize internal deliverables (e.g., statistical analysis plans). Track HTA statistics priorities and align with resources and risks.
* Identify the need for preliminary ITCs to inform value proposition, development, pricing, and commercial strategic forecast decisions.
* Lead and facilitate sharing of best practices across regions and cross-functional partners.
* Stay current with innovative techniques and robust analytics using clinical data and published information to inform pricing and market access strategy.
* Collaborate with MA Biostats for trial analyses, HTA challenges, and statistical analyses.
* Act as a Strategic Partner for HEOR & PCO and International Value & Access to ensure alignment with brand, commercial, access and evidence strategy; optimize use of comparative evidence for payer materials, regulatory dossiers, and publications.
* Provide mentoring and coaching support to junior members of evidence modelling teams and across functions.
Essential Requirements
* MSc/PhD in Statistics, Biostatistics, or related field; experience from pharmaceutical industry or life-science consultancy.
* 6-8 years relevant experience in consultancy or pharmaceutical industry in Evidence Synthesis, Health Economics, HTA, or related area.
* Strong understanding of clinical drug development and HTA-related regulations and processes.
* Local HTA experience including country HTA submissions.
* Strong understanding of statistical methodologies for ITCs and PAIC.
* Proficiency in statistical software such as R and/or SAS.
* Strong interpersonal and scientific communication skills; excellent problem-solving abilities and attention to detail.
* Ability to lead in a matrix environment and work collaboratively in interdisciplinary cross-functional teams.
Location
This role can be based in the UK (London), Basel (Switzerland), or Dublin (Ireland).
Benefits
Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: Novartis Life Handbook.
Commitment to Diversity & Inclusion
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Accessibility and Accommodation
Novartis is committed to providing reasonable accommodation to all individuals. For recruitment process accommodations, please email inclusion.switzerland@novartis.com with the nature of your request and your contact information, including the job requisition number.
Why Novartis
Joining Novartis means contributing to breakthroughs that change patients’ lives through collaboration and shared purpose. Learn more at: https://www.novartis.com/about/strategy/people-and-culture
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Job Details
* Seniority level: Mid-Senior level
* Employment type: Full-time
* Job function: Research, Analyst, and Information Technology
* Industries: Pharmaceutical Manufacturing
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