Key responsibilities:

As part of the HEOR & PCO Team:

• Develop core global Indirect Treatment Comparison (ITC) plan for HTA, payer and other Access stakeholder assessments, submissions, and negotiations. Lead publications associated with these to meet business objectives.
• Provide strategic, methodological, and analytical support to regions and top countries with adaptation of the Indirect Treatment Comparison (ITC) for local HTA submissions and support the local assessment of HTA strategy. Coordinate data requirements across evidence generations functions (Clinical Development; Medical Affairs/Biostat and HEOR & PCO) to support Pricing & Reimbursement.
• Set-up systems internally to proactively capture key HTA analytic requirements across key international markets to inform and optimize key internal deliverables e.g., statistical analysis plans. Track key HTA statistics priorities and sequence them aligning with resource availability and risks.
• Identify need for preliminary ITCs to inform value proposition, development, pricing and commercial strategic forecast and decisions.
• Lead and facilitate the sharing of best practices and key learnings across regions, countries and cross-functional partners.
• Stay on top of innovative techniques, using robust analytical techniques leveraging available clinical data and published information to inform pricing and market access strategy.
• Collaborate with the MA Biostats team for trial analyses, HTA challenges, and statistical analyses.
• Act as a Strategic Partner for key partners from HEOR & PCO and International Value & Access (Therapeutic Area Access, Pricing) to ensure alignment to brand and commercial, access and evidence strategy. Ensure optimal utilization of comparative evidence through partnership with teams generating payer & promotional materials, generating regulatory dossiers and publications.
• Provide mentoring and coaching support to junior members of evidence modelling teams and across function.

Essential requirements:

The ideal candidate will possess a strong background in statistics, with relevant experience in HTA and clinical research.

• MSc/PhD in Statistics, Biostatistics, or a 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, Health Technology Assessment, or related area
• Strong understanding of clinical drug development and HTA-related regulations and processes
• Local HTA experience including experience with country HTA submissions
• Strong understanding of statistical methodologies for indirect treatment comparisons (ITCs) and population-adjusted indirect comparison (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 but also based in Basel, Switzerland and 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 working with and providing reasonable accommodation to all individuals. If, be-cause of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

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