Vaccines Value Evidence Lead Adult Immunization and

il y a 3 semaines

Wavre, Belgique GSK Temps plein

**Site Name**: Belgium-Wavre, GSK House, Upper Providence

**Posted Date**: Jul 20 2023
**_
Join our challenge to get ahead of disease together _**

Are you ready to make a significant impact on global health?

We're seeking a passionate and experienced Value Evidence Director to join our team at GSK.

**Summary description**

The role of Value Evidence Director is essential to ensuring that vaccines that GSK brings to market are supported by scientifically credible, high quality, evidence aligned with the needs of decision makers responsible for granting access / reimbursement. As important Value Evidence Department Team member you will be accountable to lead the global value evidence strategy and delivery for vaccines for selected strategic priorities/ streams within the Essential portfolio throughout the lifecycle of the assets in alignment with the Value Evidence [VE] accountabilities around the GSK integrated asset operating model, interacting with wide range of internal and external stakeholders, to inform relevant vaccine recommendation and reimbursement.

**Your responsibilities**:

- Partner within the Value Evidence and Outcomes (VEO) organization with partners such as VEO Early, Real World Analytics teams to ensure the operational delivery of Patient Reported Outcomes (PROs), Real World Evidence (RWE), Patient Focused Development and VEO Operations as well as relevant Therapeutic Areas aligned with the Target Vaccine Profile expectations and the lifecycle of the relevant asset.
- Partner with relevant asset teams in the remit of the adult immunisation stream, as well as the related Value Evidence peers to ensure integrated approach and successful implementation and maximization for synergies and efficiency in study delivery.
- Partner with a complex set of global, regional, and local internal stakeholders including Vaccine Development Leads, Global Vaccine Commercial Leads, Epidemiology and Clinical Scientists, global and local Medical Affairs, local Market Access, regional and key LOC contributors etc. and ensure appropriate representation at project governance level.
- Support the Value Evidence Portfolio Lead in the external dialogue on the Adult Immunisation related external initiatives with co-leading several initiatives. Build deep strategic understanding of value evidence requirements for defined strategic priorities / streams (such as key assets in the remit of the adult immunisation initiative), relevant for priority markets, with recommendation and reimbursement bodies including seeking formal scientific advice to National Immunization Technical Advisory Committees (NITAGs) and Health Technology Assessment (HTA) bodies and across Industry Initiatives.
- Responsible for the design and delivery of pragmatic, prioritised health outcomes strategies and studies for development and/or marketed compounds, including health economic studies, evidence syntheses, patient reported outcome development and implementation, burden of disease and real-world effectiveness studies, run as part of or in parallel to development from Discovery through life cycle management.
- Lead scientific robust value evidence studies in collaboration with direct report and broader VEO organization (e.g., cost-of-illness, resource utilization, utility and quality of life assessments, Patient Reported Outcomes (PROs), Real World Evidence (RWE), economic and public health impact modelling, indirect study comparisons, etc) ensuring scientific robustness and compliance with necessary regulations for quality and disclosure.
- Lead annual budget forecasting and activity prioritization for defined streams while effectively managing projects and budgets for Human Subject Research (HSR) and non-HSR activities.
- Lead, develop and support potential direct report(s)
- Lead potential vendors, agency workers allocated to the stream in ensuring successful implementation of respective Value Evidence Plans aligned to the overall Neisseria portfolio strategy.
- Integrate excellent understanding of the evolving global NITAG, Health Technology Assessment, policy decision maker and payer environment, including recommendation, reimbursement, pricing, and access.


**_ Why you?_**

**Basic Qualifications**:

- Masters level or equivalent experience in health outcomes or relevant areas of specialisation
- Specific training / meaningful experience in at least 2 areas (health policy, reimbursement / access, health economics, modelling, patient reported outcomes, psychometrics, clinical trial design, observational research, epidemiology, statistics).

Job-Related Experience:

- At least 5 years’ experience in a health economist, market access or related function (consulting, pharmaceutical industry, academics), preferably including above country level experience
- Educational background with technical expertise consistent with scientific project planning, implementation, and delivery of evidence.
- Knowledge of global reimbursement processes /

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