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For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain market positioning. The role of 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.
Job Responsibility
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, in adherence to SOPs
Identify resources, references and analyses to inform scientific design and advise internal experts.(medical affairs, clinical, commercial/market access) and external experts as needed in support of the asset team
Translate 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 clinicians and HTA requirements, and their acceptance of different types of evidence and impact of that evidence to their decision making
Collaborate with internal teams and participate in best practice sharing sessions across the non-interventional study 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 relationships with external thought leaders to ensure appropriate methods and research agendas are applied, in accordance with GSK policies.
Requirements
MSc, or equivalent in health outcomes, health economics, epidemiology, pharmacy, health or life sciences
3+ years of experience working in the pharmaceutical industry, preferably in a multi-national company
Experience in planning and delivering individual projects, managing budgets and working within a matrix setting
A history of designing a variety of RWE studies including prospective observational studies, cross-sectional and retrospective cohort studies, chart reviews, and database analyses
Proficiency in utilizing evidence for the development of HTA submissions, reimbursement and/or medical engagements
A track record of delivering robust payer evidence and credibility to engage meaningfully with external experts and leaders in the field
Expertise with the diversity and complexity of healthcare markets, health technology assessment agencies, and reimbursement decision making globally, in region and local markets
Experience in communicating technical and complex concepts and results to various audiences to impact decision-making
Experience in oncology.
Nice to have
Advanced scientific degree, e.g. PhD, PharmD or equivalent in Health Economics, 0utcomes Research, Epidemiology or similar
Experience in gynecological cancers
Experience in Global and Country roles in oncology
Launch experience.
What we offer
Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes
Health care and other insurance benefits (for employee and family)