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Site Name: UK - London - New Oxford Street
Posted Date: Apr 28 2025
Job Purpose
Ensure the development of appropriate regional regulatory strategy(ies) and their execution for assigned asset(s) consistent with the strategic activities for GSK's Established Products (EP) portfolio. Maintain/ensure compliance with internal GSK processes/policies and regional regulatory requirements.
Key Responsibilities
* Accountable to the Senior/Executive Director for developing and delivering regional and/or global regulatory strategies.
* Lead interactions with local/regional regulatory authorities.
Additional responsibilities include implementing regional strategies, leading regulatory interactions, ensuring compliance, advocating persuasively to senior leaders and authorities, and assessing potential in license molecules.
Why you?
Basic Qualifications:
* Bachelor's degree
* 5+ years industry regulatory affairs experience
* 5+ years leading matrixed teams across global regions
Preferred Qualifications:
* PhD or Master's in life sciences or pharmacy
* Strong technical knowledge of regulatory compliance
* Experience with regulatory officials and advocacy
* Extensive drug development regulatory experience
* Proven leadership in regional development, submission, and approval activities
* Knowledge of clinical trial and licensing requirements globally
Why GSK?
GSK is a global biopharma company committed to uniting science, technology, and talent to combat disease, focusing on vaccines, medicines, and the immune system. We value our people and aim to create an inclusive environment where everyone can thrive. Join us in our journey to get Ahead Together.
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