Associate Director, Global Real-World Evidence and Health Outcomes Research, Neisseria Scientist

EngineeringUK; London; On-site; GBP 60,000 - 100,000

Job description

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Associate Director, Global Real-World Evidence and Health Outcomes Research, Neisseria Scientist

Sector: Legal, Research and Development, Science and Pharmaceutical
Role: Associate
Contract Type: Permanent
Hours: Full Time

Site Name: USA - Pennsylvania - Upper Providence, Belgium-Wavre, UK - London - New Oxford Street
Posted Date: Mar 5 2025

For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement, and maintain market position. Specifically, evidence must be maintained throughout the product lifecycle as standard of care changes, new competitors are introduced, and patents expire on existing competitors. The landscape is evolving quickly as trials demonstrating efficacy in an area of unmet need may receive expedited review, or orphan product status designation which affects both GSK and competitors launch timelines and approval requirements. More and more of our customers are developing sophisticated internal health outcomes capabilities and access to real world data that can be used to better understand unmet needs and real-world effectiveness of our medicines. We need to better understand how our customers define value and to effectively collaborate with them to ensure we are generating value evidence data that includes real world evidence and cost effectiveness analysis that is impactful for payers, health systems, providers, and patients.

The role of Associate Director, Global Real-World Evidence & Health Outcomes Research Scientist is critical to achieving this ambition by supporting asset teams to ensure that each medicine GSK brings 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 role is critical to support the alignment of evidence with evidentiary requirements of customers responsible for marketing authorization, recommendation and reimbursement leading to successful patient access, product use, and commercial success.

Responsibilities

The role will report directly into the Global Real-World Evidence & Health Outcomes Research Lead for a complex priority asset and will have expertise in real-world evidence and other non-interventional study methods. The role will be a key member of the asset team and other relevant matrix leadership teams. The Associate Director, Global Real-World Evidence & Health Outcomes Research Scientist will be accountable for engaging closely with medical and matrix stakeholders and partner effectively in data generation plan (DGP) planning, design, execution, translation, and dissemination at the study level for the asset.

• Plan, design and execute multiple studies for a given asset and manage timelines, deliverables, and budget.
• Assure quality of deliverables, including review and sign off project specifications, protocols, data analysis plans, final study reports, abstracts, posters and manuscripts, adherence to SOPs.
• Identify resources, references and analyses to inform scientific design and advise internal experts (clinical, commercial/market access) and external experts as needed in support of the asset team.
• Translate 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.
• Develop and maintain a good working knowledge of real-world data resources, existing partnerships and public initiatives and become the point person for select sources to advise on their suitability to address given research questions.
• Develop a deep understanding of customers' needs, including HTA requirements, as well as the acceptance of RWE or economic evidence and impact on the decision making of different customers (reimbursement, medical societies, physicians).
• Collaborate with internal teams and participate in best practice sharing sessions across NIS organization.
• Build 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.
• Ensure key stakeholders including TA aligned business leaders are regularly updated on plans through periodic reporting.
• Develop excellent working relations with external thought leaders to ensure appropriate methods and research agendas are applied, in accordance with GSK policies.

Basic Qualifications

• MSc, or equivalent in health outcomes, patient reported outcomes, health economics, epidemiology, pharmacy, health or life sciences.
• Minimum 1-3 years' experience working in the pharmaceutical industry, preferably in a multi-national 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.

Preferred Qualifications

• Advanced scientific degree, e.g. PhD, PharmD in Health Outcomes or related Science.
• Preferred 3-4 years of experience, Global Real-World Evidence & Health Outcomes.
• Direct Payer experience.
• Launch experience.

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organization where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged, and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

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