Live opening · Posted 1 day ago

Director, Global Health Outcomes, ViiV Healthcare

GSK · 2 Locations
Workday
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At a glance

The key details from the original listing.

Posted 1 day ago
CompanyGSK
Location2 Locations
SourceWorkday
ListedPosted 1 day ago

About the role

Description supplied by the original job listing.

Business Introduction:
We are a specialist pharmaceutical company 100% dedicated to developing medicines to treat and prevent HIV. Born out of a partnership between GSK and Pfizer in 2009, with Shionogi joining in 2012, our ambition is to end the HIV epidemic.
As the pioneers in HIV innovation, we constantly look to push the boundaries of science to develop medicines that can change lives and give people more choice. Beyond our medicines, we are proud of our deep connection with the HIV community and work with partners to advance research and development, address HIV-related stigma, increase access to our medicines and provide funding and support to local community organisations to support their efforts in the HIV response.
We are ViiV Healthcare. Here until HIV and AIDS are not.
Position summary:
You will join the Global Health Outcomes function within ViiV Healthcare and lead the design and delivery of robust, decision-relevant evidence for an assigned portfolio of HIV treatment and prevention medicines, whether in clinical development or already established in the market.
You will shape integrated health economics and outcomes research (HEOR) and value evidence strategies spanning real-world evidence (RWE), clinical outcome assessments (COAs), evidence synthesis and economic modelling. Working closely with research and development, medical affairs, market access, commercial and external stakeholders, you will build fit-for-purpose evidence plans that answer the questions decision-makers care about most.
This role combines scientific leadership with genuine strategic influence. You will set a forward-looking clinical outcome assessment (COA) and patient-centred outcomes (PCO) strategy, embedding differentiated endpoints that demonstrate meaningful value to patients, clinicians, payers and healthcare systems. Partnering with asset teams, whether shaping the evidence package for innovative medicines in development or strengthening the value story for established medicines in a competitive market, you will ensure every ViiV medicine is supported by scientifically credible, high-quality evidence that meets the requirements of regulators, health technology assessment (HTA) bodies and payers. Your work will directly inform product positioning, value propositions and value-based pricing, and help secure patient access, appropriate use and commercial success. Success in this role requires strong scientific judgement and the ability to lead and influence in a complex matrix environment.
Key responsibilities:
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
Define the integrated evidence strategy for your assigned assets, bringing together patient-focused outcomes, economic models and real-world evidence to meet regulatory, payer and other stakeholder needs
Represent value evidence in cross-functional integrated evidence teams and decision forums, influencing the key decisions for your assets, whether in development, at launch or in market
Define a Clinical Outcomes Assessment strategy for each asset, ensuring alignment with disease area needs, regulatory expectations, and payer evidence requirements
Drive the identification and integration of differentiated endpoints to strengthen value propositions across assets
Guide the development and use of fit-for-purpose instruments and endpoint frameworks, supporting consistency and scalability across the HIV portfolio
Partner with patient outcomes, clinical development, medical affairs and market access to translate strategy into study design, endpoints and evidence plans
Engage external stakeholders (payers, HTA bodies, guideline groups and academic partners) to ensure evidence meets decision-maker needs
Oversee the quality, compliance, budget and delivery of health outcomes and real-world evidence studies for your assets, whether generating pre-launch evidence or post-launch evidence that sustains access and differentiation
Build strong relationships with country, regional and global teams across medical, market access, R&D and commercial, ensuring global evidence plans translate into local access and medical priorities
Additional information:
Reporting line: Senior Director, Global Health Outcomes, ViiV Healthcare
Primary location: GSK London HQ (UK)
Secondary location: Durham (NC, US)
Presence onsite: hybrid
Business travel: limited
People management involved: N/A
Why You?
Basic Qualifications:
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
Advanced degree (Master’s or equivalent) in health outcomes, health economics, epidemiology, pharmacy, public health, or a related discipline
Significant pharmaceutical industry experience in health outcomes, real-world evidence, clinical outcome assessment strategies, market access or value evidence roles
Demonstrated experience designing strategic evidence generation to be utilized in the development of reimbursement or HTA submissions and/or medical engagement across multiple markets
Experience contributing to the development, validation, or implementation of COA instruments or digital measures in clinical trials
Knowledge of the diversity and complexity of healthcare markets, health technology assessment agencies and reimbursement decision-making at global, regional and local levels
Experience delivering studies and communicating their findings in a complex, fast-paced matrix organisation
Strong scientific judgement in study design, patient-reported outcomes, and evidence synthesis
Excellent communication and influencing skills, including ability to translate data into strategic insights and business impact
Preferred Qualifications:
If you have the following characteristics, it would be a plus:
PhD or other advanced research degree in a relevant discipline
Direct experience with global launches and above-country evidence strategy
Experience leading COA instrument development or cross-cultural adaptation, from concept elicitation through to psychometric validation
Track record of peer-reviewed publications or scientific leadership
Prior experience engaging with HTA agencies, guideline committees or payers
Experience managing external vendors and large multi-country studies
Health economics and outcomes research experience in HIV treatment and/or prevention, or in another chronic disease area with innovative or long-acting treatment options
Methods expertise to deliver robust payer evidence, and the credibility to engage meaningfully with external experts and leaders in the field
What we value in you:
You communicate clearly and respectfully, focus on patients and work with integrity. You are curious, pragmatic and confident explaining technical findings to non-technical audiences. You bring people together, build trusted relationships, influence decisions across disciplines and grow the capability of those around you.
How to apply
Please submit your CV together with a brief statement outlining how your experience aligns with the role’s responsibilities and qualification requirements. We welcome applications from people of all backgrounds who share our commitment to inclusion and collaboration.
Application end date
Sunday, November 1st, 2026 – EOD CET
#LI-GSK
Skills
Cross-Functional Leadership, Digital Fluency, Enterprise Thinking, Evidence Based Decision Making, Flexible Mindset, High Impact Communication, Launch Excellence, Patient Journey
Why Us?
At ViiV Healthcare, we will not rest until we leave no person living with HIV behind. Until the 40 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV.
We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between GSK and Pfizer in 2009, with Shionogi joining in 2012, we are determined to help end the HIV epidemic. We are guided by our mission to leave no person living with HIV behind and it is this mission that unites our employees located across the globe. We combine expertise in research, manufacturing, policy and more to push the boundaries of what people think is possible in HIV treatment and care. As a result of our connection with GSK, we are able to draw on their proud history and resources. This means that you would receive all the employee benefits offered by GSK.
Living our mission of leaving no person living with HIV behind means keeping inclusion and diversity at the heart of everything we do - from our breakthrough innovation, to our diverse portfolio of medicines as well as the work we do to partner with HIV communities.
Having a truly inclusive cultur

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