Associate Director, Global Real-World Evidence Lead

3 weeks ago


London, Greater London, United Kingdom GlaxoSmithKline Full time
About the Role

We are seeking an experienced Associate Director to lead our Global Real-World Evidence and Health Outcomes Research team. As a key member of our organization, you will be responsible for developing and executing strategies to generate high-quality, evidence-based data to support our medicines and drive business success.

Key Responsibilities
  • Plan, design, and execute multiple studies for a given asset, managing timelines, deliverables, and budget.
  • Assure 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.
  • 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 to the decision-making of different customers (reimbursement, medical societies, physicians).
  • 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.
  • Develop excellent working relations 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, 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.
  • 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.


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