- Analyze the local RWE landscape together with the local cross-functional team and Region/Global RWE team. Identify potential gaps, anticipate potential access challenges, and needs for the next 1-3 years, and set up a plan to meet those needs.
- Align with Early Value Access Lead and Medical New Products Lead the local RWE generation plan within the launch plans and the clinical trial prioritization plan for the asset brands.
- Understand the evidence needs and make recommendations on fit-for-purpose data and analytics solutions.
- Responsible for the tactical execution of RWE strategy and plans for Novartis products.
- Working with external costumers to execute applicable projects
- Conduct routine literature review in relate therapeutic area to understand Novartis product and comparator status.
- Provide input to global/region regarding data generation for pipeline.
- Build experience in evidence generation methodologies and their processes at Novartis and its legal and regulatory framework.
- Partner with cross-functional teams in the development of evidence to support reimbursement dossiers and formulary listing.
- Lead and coordinate activities for the publication (e.g., papers, congress presentations) of the evidence generated and communicate this evidence with external stakeholders.
- Develop and support RWE projects management with high standards of operational excellence.
- Networks effectively across Novartis and wider forums to identify opportunities for
collaboration and to identify and leverage best practices across the function.
- Lead the RWE capability building at a local level.
- Interact with others in a positive and constructive way, being open to diversity and aligned with corporate guidelines, in order to guarantee Novartis has a working environment free from all forms of discrimination and harassment as well as contributing to a positive and inclusive working environment.
- Work within Integrity and Compliance policies and ensure those around him/her do the same, complying with job Excellence Standards to contribute to the alignment with Novartis Global procedures and objectives.

Key performance indicators:

• Quality and timeliness of evidence plan deliverables
• Publications and congress presentations
• Readiness & Quality of /RWE strategy
• Feedback from internal and external stakeholders

Minimum Requirements:
Work Experience:

• At least 3 years of experience of technical expertise and research methodological understanding in academic or pharmaceutical industry
  • Deep understanding and experience in RWE projects
  • Technical expertise and research methodological understanding to include statistical analysis, clinical studies, patient surveys, observational/epidemiologic research, and health technology or other outcome assessment.
  • Knowledge of both scientific and operational aspects of clinical drug development in all phases, including post-marketing and RWE.

Skills:

• Good understanding of drug development, market access process
• Project Management
• Data analysis & critical thinking
• Expertise in clinical investigation methodology, epidemiology, and biostatistics

Languages :

• English
• Portuguese

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Division
International

Business Unit
Innovative Medicines

Location
Portugal

Site
Sintra

Company / Legal Entity
PT05 (FCRS = PT005) PT Pharma

Functional Area
Market Access

Job Type
Full time

Employment Type
Regular

Shift Work
No