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GSK R&D Global Regulatory Affairs Virtual Panel
Join our R&D GRA teams!
Grab your lunch or coffee for a conversation with our leaders and learn more about our organization and the opportunities we have to offer you.
If you want to be part of a leading healthcare organization with insights into the science of our medicines & vaccines to safely reach the right patients faster, a role in our Global Regulatory Affairs area might be the perfect place for you!
It’s here that we advise on legal and scientific requirements; collect, collate and evaluate scientific data in order to confirm the quality, safety and efficacy of our drugs – while keeping track of changing global health authority requirements.
At GSK, we believe that biopharmaceutical medicines are vital to achieving our ambitions in immuno-oncology and other immunologically driven diseases. We unite science, talent, and technology to get ahead of disease together. Our state-of-the-art end-to-end capability delivers efficient discovery of antibody molecules that are selected and engineered for rapid development so that, together with our therapy area partners, we discover, develop and manufacture a novel portfolio of exciting medicines to benefit patients around the world.
We are creating an environment of belonging, where diversity of people and thoughts are valued and we feel we can be ourselves. We support your health and wellbeing while encouraging your continuous development. It’s all part of the deal we make with you when you work here – we want you to fulfill your potential and accomplish great things, so we support you to do so.
Join us for an hour to hear from our leaders about their career journeys and the culture we are creating at GSK GRA. You'll also have an opportunity for Q&A.
Note: Your identity will be anonymous to other participants unless posting a question to our Q&A.
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We are on the cutting edge of new modalities while having the knowledge necessary to rapidly deliver new medicines to patients. - Tracy, Manager, Regulatory Affairs
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