Site Name: USA - Pennsylvania - Upper Providence, Cambridge Park Drive, Collegeville TSA, USA - Maryland - Rockville
Posted Date: Aug 28 2024
Job PurposeEnsure the development of appropriate regional regulatory strategy(s) and their execution for assigned asset(s) consistent with Medicines Development Strategy. This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process / policy and with regional regulatory requirements to deliver the best possible labeling, commensurate with the available data. Key ResponsibilitiesAccountable to GRL and Global Regulatory TA Head for development of appropriate regional and/or global regulatory strategy(ies) and for delivery according to plans. The Regulatory Director may be the single point of contact on assigned asset(s), responsible for regional and global regulatory strategy(ies). In conducting role, planning will be on a multiple year horizon, with delivery requiring extensive matrix working within GSK to VP level and representing GSK with at least the local regulatory agency. Work closely with local / regional commercial team to secure best possible labelling commensurate with the available data. Lead interactions with local / regional regulatory authorities. Ensure the regulatory strategy will deliver the needs of the local region(s), taking in to account the needs of other regions globallyImplement the regional strategy(s) in support of the project globallyLead regulatory interactions and the review processes in local regionEnsure appropriate interaction with regional commercial teams in local regionEnsure compliance with regional requirements at all stages of product life from C2MDIdeally able to advocate persuasively approaches to senior leaders in GSK and in Health Authorities Capable of providing assessment of potential in license molecules Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals:
Bachelor's degreeExperience in Regulatory Affairs within a pharmaceutical organizationExperience working with Global Health Authorities and submissions for Phamaceutical productsPreferred Qualifications: If you have the following characteristics, it would be a plus:
PhD or Masters' degree in life sciences or pharmacyStrong technical knowledge required to be able to assess regulatory compliance of productsAbility to interact with regulatory officials and support advocacy initiativesPlease 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.
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