Global Value Evidence Associate Director
il y a 1 semaine
Site Name:
Belgium-Wavre, GSK House
Posted Date:
Mar
Are you looking for a high-profile health outcomes role that shapes solid evidence generation for our medicines across the region? If so, this
Global Value Evidence Associate Director Pneumococcal Multiple Antigen Presenting System (MAPS) Vaccines role could be an exciting opportunity to explore.
As Global Value Evidence Associate Director pneumocccal Multiple Antigen Presenting System (MAPS) Vaccines you are accountable for supporting the global value evidence strategy and delivery (health outcomes, economics, patient reported outcomes, stakeholder insights including payer, HTAs and patients, and real world evidence) for the pneumococcal MAPS assets in Development and in alignment with the Value Evidence (VE) accountabilities around the GSK integrated asset operating model.
Collaborative working with diverse business partners across R&D, commercial and regional and affiliate VE, health outcomes and market access teams will be critical to ensure optimal evidence generation strategies are in place.
These responsibilities include some of the following:
- Contribute to the development of critical vaccines development activities which include: the Integrated Evidence Plan (with a focus on the needs of payers, providers and patients), the Vaccines Profile, and the Value Proposition.
- Contribute to the development of the global Value Evidence Plan comprising the set of claims / messages to be supported by value evidence studies; definition of markets requiring payer scientific advice; program of studies to support key value claims, reflecting the needs of key affiliates and delivering on the vaccine profile ultimately informing vaccine recommendation and reimbursement.
- In collaboration with cross functional stakeholders (Clinical, Real World Data analytics, Real World Evidence and Epidemiology, Patient centric outcomes, Medical affairs and Commercial, Governmental Affairs and regional / affiliate VE teams), lead studies and implement and deliver specific research plans/protocols including the development of health economic models, burden of illness studies, observational research, patientreported outcomes instruments, payer or patient insight studies to inform VE research.
- Inform clinical trial design to capture the economic and humanistic measurements required to deliver a vaccine with differentiated value.
- Conduct and lead scientific engagements with external experts, HTA bodies, payers and patients to inform the Value Evidence Plan and Research activities.
- To effectively lead and deliver outsourced projects with external contract research organisations/suppliers
- Bring expertise to strategic discussions regarding the evidence requirements to support recommendation and reimbursement submissions globally.
- Support regulatory interactions with a focus on the patient reported outcome data, labelling and potential for inclusion in indication
- Lead or collaborate with other functions, such as Market Access, Medical Affairs or Commercial, on the direct or indirect collection of insights from patients, physicians, providers, and payers.
- Support projects as required through key internal development milestones and communicate the evidence generation plans effectively to secure resources, funding, and organizational alignment.
_ Why you?_:
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
- 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).
- Jobrelated experience: At least 4 years experience in a health economist, market access or related function (consulting, pharmaceutical industry, academics), preferably including above country level experience and vaccine experience
- Educational background with technical expertise consistent with scientific project planning, implementation, and delivery of evidence.
- Drug development experience including early planning, clinical programmes, and/or launch or post marketing experience.
- Knowledge of global reimbursement processes / evidence requirements to inform access decisions for vaccines (preferred) or pharmaceuticals. Experience of reimbursement / HTA submissions is a plus.
- Proficient in managing multiple projects, budgets, and matrix interactions (internal / external consistent with each research project).
- Authored publication in a relevant field.
Preferred Qualifications:
If you have the following characteristics, it would be a plus:
- Experience in pneumococcal disease/vaccination.
- PhD in a relevant discipline.
- Programming skil
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