Job Details

ID #52678625
State Pennsylvania
City Collegeville
Full-time
Salary USD TBD TBD
Source GlaxoSmithKline LLC
Showed 2024-10-10
Date 2024-10-11
Deadline 2024-12-09
Category Et cetera
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Associate Director, Real World Data Strategy and Partnerships

Pennsylvania, Collegeville, 19426 Collegeville USA
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Reference #: 403491

Site Name: USA - Pennsylvania - Upper Providence, UK - London - New Oxford Street

Posted Date: Sep 30 2024The 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 Biostatistics, R&D tasked with realising the potential of RWD and RWE. The vision is to build an 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 role, reporting to Sr Director of RWD Strategy and Partnerships, will give you the opportunity to drive forward this vision through leading efforts within the Respiratory and Immunology portfolio from Research through Development and Medical Affairs, as well as contributing to building the enterprise-wide RWD framework. The role will have the following responsibilities:

Lead periodic reviews of data needs across the respiratory and immunology 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 cross-functional team, including R&D Policy, Advocacy and External Engagement experts, Research Units, Biostatistics, Medical, Regulatory, Clinical, global and regional medical teams to realise enterprise vision of RWD/E.

Ensure partnerships are optimised internally via knowledge management and cross-matrix collaboration.

Lead RWD acquisition for key individual activities as identified by teams as part of evidence generation plans 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.

Assess data for its suitability for use in 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.

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 hands-on with data exploration, especially for newer data sources.

Promote the data driven development culture within R&D and beyond; be ambitious for driving use cases of maximising value of data and tech investments across the enterprise

Basic Requirements

Advanced degree (MSc) or higher in Public Health, Epidemiology, Health Informatics, Statistics, HEOR or Life Sciences

Supplier relationship management experience at operational and strategic levels

Experience of collaborating within a global matrix team, building consensus and encouraging diverse inputs

Experience in research and development, preferably in respiratory, immunology or hepatology

Significant pharmaceutical industry experience that includes deep knowledge of RWE study designs and medicine development/reimbursement processes

Preferred ExperienceExperience and practical knowledge of statistical/analytic software (e.g., SAS, R, IHD)

Solid understanding of technology requirements for ingesting and hosting external RWD.

Experience with common data ontologies

A good understanding of healthcare systems in multiple geographies (e.g. US, EU and Asia Pacific)

Big-picture and visionary thinker to drive strategic vision of partnerships, with facilitation and strategy formulation experience aligned with RWE / R&D priorities.

Understanding of the external regulatory, data governance and payer environments and suitability of RWD for research for external audiences

Demonstrated hands n 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

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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 organisation 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.If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).Important notice to Employment businesses/ Agencies

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