Associate Director, Real World Data

il y a 1 semaine


Wavre, Wallonie, Belgique GSK Temps plein

Site Name:
UK - London - Brentford, USA - Pennsylvania - Upper Providence, Wavre

Posted Date:
Jun 7 2023

372337 Associate Director, Real World Data (RWD) Strategy and Partnerships


GSK's Value Evidence and Outcomes (VEO) team play a crucial role in ensuring that treatments and vaccines that GSK aims to develop and commercialise are supported by scientifically credible, high-quality evidence aligned with the needs and acceptability criteria of key external decision makers including regulators, payors and physicians.


The use of real-world data (RWD) to demonstrate this value proposition through real world evidence (RWE) is becoming an increasingly important component of the integrated evidence planning process.

Coupled with this, RWD is being used in an increasing number of areas across the medicine and vaccine development lifecycle from early discovery to market access and expertise in selecting the right data source for the right question is in demand.


This increased demand both internally and externally for high quality, robust RWE from RWD requires GSK to access and partner with the external RWD environment to ensure evidence generation is held up to the highest possible standards.

The RWD Strategy team is a small team in VEO tasked with realising the potential of RWD and RWE.

The vision is to build an interconnected RWD ecosystem to drive expanded use, enabling better evidence generation and decision making across R&D.

The team aims to be leaders in building innovative partnerships and contributing to the future evolution of high quality RWD for research.


This exciting role, reporting to the Sr Director of RWD Strategy and Partnerships, will give you the opportunity to drive forward this vision through leading efforts within the Infectious Disease and Vaccines portfolios, as well as contributing to building the enterprise-wide RWD framework.


In this role you will

  • Lead periodic reviews of data needs across the infectious disease and/or vaccine portfolio and identify changes in strategy to address evolving business needs.
  • Define key RWD capability requirements to advance RWE generation within the portfolio and collaborate in a crossfunctional team, including R&D Policy, Advocacy and External Engagement experts, Experimental Medicines Unit, Medical, Regulatory, Clinical, Commercial, VEO global and regional teams to realise enterprise vision of RWD/E.
  • Ensure partnerships are optimised internally via knowledge management and crossmatrix collaboration.
  • Lead RWD acquisition for key individual studies defined in Integrated Evidence Plans (IEPs) and the development of larger RWD initiatives, including: Data landscaping and assessments; recommending RWD sources for insourced and outsourced studies; identify additional RWD and capability needs for VEO.
  • Assess data for its suitability for use in externally acceptable evidence generation with consideration for eventual study design. Conduct quantitative assessment of metadata for completeness and qualitative assessment on provenance, representativeness and reliability for research. Match these findings with the overall integrated evidence strategy (IEP) to ensure selected data will help generate evidence that meets overall product development goals.
  • Work in partnership with Real World Analytics (RWA) to ensure optimal investment in data purchases and streamlined use of data for evidence generation and rapid data queries. This will include being very handson with data exploration, especially for newer data sources.

_ Closing Date for Applications:
June 28th, 2023 (COB)_

Please take a copy of the Job Description, as this will not be available post closure of the advert.#LI-GSK

_ Why you?_

Qualifications & Skills:

We are looking for professionals with these required skills to achieve our goals:

  • Advanced degree (MSc) or higher in Public Health, Epidemiology, Health Informatics, Statistics, HEOR or Life Sciences
  • Supplier relationship management experience at operational and strategic level
  • Ability to effectively communicate and influence key stakeholders at all levels of the organization, both internally and externally
  • Ability to successfully collaborate within a global matrix team, building consensus and encouraging diverse inputs
  • Experie
nce in research and development, preferably in the infectious disease or vaccines areas

  • Significant pharmaceutical industry experience that includes deep knowledge of RWE study designs and medicine development/reimbursement processes
  • Demonstrated hands on experience in real world evidence study design and/or analysis with deep understanding on how to work with real world data and assess quality and reliability
  • Understanding of the external regulatory, data governance and payer environments and suitability of RWD for research for external audiences

Preferred Qualifications & Skills:

If you have the following characteristics, it would be a plus:

  • Experie


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