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Director, Global Real-World Evidence and Health Outcomes Research Lead
1 month ago
We are seeking a highly skilled and experienced Director, Global Real-World Evidence and Health Outcomes Research to join our team at GSK. This role will play a critical part in driving our ambition to get ahead of disease together by supporting asset teams to ensure that each medicine we bring to market is supported by scientifically credible, high-quality evidence that drives competitiveness and strong evidence-based product positioning, value propositions, and value-based pricing.
The successful candidate will have expertise in real-world evidence and other non-interventional study methods, with a strong track record of planning and delivering individual projects, managing budgets, and working within a matrix setting. They will be accountable for engaging closely with medical and matrix stakeholders and partnering effectively in data generation plan (DGP) planning, design, execution, translation, and dissemination at the study level for the asset.
The key responsibilities of this role include:
- Planning, designing, and executing multiple studies for a given asset and managing timelines, deliverables, and budget
- Assuring quality of deliverables, including review and sign-off of project specifications, protocols, data analysis plans, final study reports, abstracts, posters, and manuscripts, adherence to SOPs
- Identifying resources, references, and analyses to inform scientific design and advising internal experts (clinical, commercial/market access) and external experts as needed in support of the asset team
- Translating identified needs for evidence into study concepts in alignment with strategic objectives and vision for the asset, e.g., development of study protocols and proposing innovative and cost-effective ways of developing and executing studies
- Developing and maintaining a good working knowledge of real-world data resources, existing partnerships, and public initiatives and becoming the point person for select sources to advise on their suitability to address given research questions
- Developing a deep understanding of customers' needs, including HTA requirements, as well as the acceptance of RWE or economic evidence and impact to the decision-making of different customers (reimbursement, medical societies, physicians)
- Collaborating with internal teams and participating in best practice sharing sessions across NIS organization
- Building strong working relationships with stakeholder groups across medical, market access, R&D, and commercial to ensure strategic alignment and optimal cross-functional collaboration and communication
- Ensuring key stakeholders, including TA aligned business leaders, are regularly updated on plans through periodic reporting
- Developing excellent working relations with external thought leaders to ensure appropriate methods and research agendas are applied, in accordance with GSK policies
We are looking for professionals with the following required skills to achieve our goals:
- MSc or equivalent in health outcomes, patient-reported outcomes, health economics, epidemiology, pharmacy, health, or life sciences
- Minimum 3 years' experience working in the pharmaceutical industry, preferably in a multinational company
- Demonstrated ability to plan and deliver individual projects, manage budgets, and work within a matrix setting
- Experience with a variety of study designs, i.e., RWE studies including prospective, cross-sectional, and retrospective cohort studies
- Applied experience in utilizing evidence for the development of HTA submissions, reimbursement, and/or medical engagement
- Methods expertise to effectively deliver robust payer evidence and credibility to engage meaningfully with external experts & leaders in the field
- Knowledge of the diversity and complexity of healthcare markets, health technology assessment agencies, and reimbursement decision-making globally, in region, and in local markets
- Understanding of how health economics, health outcomes, comparative effectiveness research, PRO research, and the use of PRO instruments can be applied at local decision-making levels, including support of clinical practice
- Ability to communicate technical and complex concepts and results effectively to various audiences to impact decision-making
- Self-motivated with the ability to work independently and develop credibility with colleagues throughout the enterprise
If you have the following characteristics, it would be a plus:
- Advanced scientific degree, e.g., PhD, PharmD, or equivalent in health outcomes or similar
- Experience in above-country and in-country roles
- Direct Payer experience
- Launch experience
We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities, contact us on Ukdiversity.recruitment@gsk.com or 0808 234 4391.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment.
