Director
Pobo?ka: UK – London – New Oxford Street, Durham Blackwell Street, Italy - Siena, Stevenage, Switzerland - Zug, Upper Providence, USA - Massachusetts - Waltham
Datum zve?ejn?nÃ: Jan 5 2026
Director, Global Regulatory Affairs Are you passionate about making a difference in global healthcare? At GSK, we are dedicated to improving lives by delivering innovative medicines and vaccines. As a Director of Regulatory Affairs, you will play a pivotal role in shaping regulatory strategies that ensure the availability of safe and effective treatments worldwide. Join us and be part of a team committed to creating healthier communities. Job Purpose Accountable to GRL and Global Regulatory TA Head, the Director of Regulatory Affairs will lead the development of regional / global regulatory strategies and their execution for assigned asset(s) aligned with the overall Medicines Development Strategy. Planning will be on a multiple year horizon, with delivery requiring extensive matrix leadership within GSK to VP level and representing GSK with local regulatory agency. This role works closely with local / regional commercial teams to secure best possible labelling commensurate with the available data. Lead interactions with local / regional regulatory authorities. Key Responsibilities Ensure the regulatory strategy will deliver the needs of the local region(s), considering the needs of other regions globally. Implement the regional strategy(s) in support of the project globally. Lead regulatory interactions and the review processes in local region. Ensure appropriate interaction with regional commercial teams in local region. Ensure compliance with regional requirements at all stages of product life. Advocate persuasive approaches to senior leaders in GSK and in Health Authorities. Capable of providing assessment of potential in license molecules.
Why You? Basic Qualifications Bachelor’s degree in Biological or Healthcare Science, with previous experience in similar strategic international regulatory affairs positions. Extensive Experience in regulatory affairs across all phases of drug development. Proven track record in leading regional development, submission, and approval activities. Experience working on clinical trial and licensing requirements in major countries.
Preferred Qualifications PhD in Biological or Healthcare Science. Experience with projects involving little or no precedence in regulatory affairs. Expertise in developing product or therapeutic knowledge in new areas. Familiarity with digitalization in regulatory strategy to enhance decision-making and innovation. Proven ability to deliver creative solutions to regulatory challenges while ensuring compliance. Exceptional communication and leadership skills, with the ability to build strong networks and influence stakeholders.
The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.
If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.Pro? GSK? Spojenà v?dy, technologie a talentu, abychom spole?n? p?edcházeli nemocem. GSK je globálnà biofarmaceutická spole?nost, jejÃmž cÃlem je spojit v?du, technologii a talent, aby spole?n? p?edstihla nemoci. NaÅ¡Ãm cÃlem je pozitivn? ovlivnit zdravà 2,5 miliardy lidà do konce desetiletà jako úsp?Å¡ná, rostoucà spole?nost, kde lidé mohou prosperovat. P?edcházÃme nemocem a lé?Ãme je inovacemi ve specializovaných lécÃch a vakcÃnách. Zam??ujeme se na ?ty?i terapeutické oblasti: respira?nÃ, imunologie a zán?ty; onkologie; HIV; a infek?nà nemoci – abychom mohli ovlivnit zdravà ve velkém m??Ãtku. Lidé a pacienti po celém sv?t? spoléhajà na léky a vakcÃny, které vyrábÃme, proto jsme odhodláni vytvá?et prost?edÃ, kde naÅ¡i lidé mohou prosperovat a soust?edit se na to, co je nejd?ležit?jÅ¡Ã. NaÅ¡e kultura být ambicióznà pro pacienty, odpov?dnà za dopad a d?lat správné v?ci je základem toho, jak spole?n? dodáváme výsledky pro pacienty, akcioná?e a naÅ¡e lidi. V??Ãme v agilnà pracovnà kulturu pro vÅ¡echny naÅ¡e role. Pokud je pro vás d?ležitá flexibilita, povzbuzujeme vás, abyste prozkoumali s naÅ¡Ãm náborovým týmem, jaké jsou možnosti. Pokud pot?ebujete jakékoli úpravy naÅ¡eho procesu, které by vám pomohly ukázat vaÅ¡e silné stránky a schopnosti, kontaktujte nás na UKRecruitment.Adjustments@gsk.com, kde si m?žete také požádat o telefonát. Vezm?te prosÃm na v?domÃ, že pokud se váš dotaz netýká úprav, nebudeme schopni vám prost?ednictvÃm t?chto kanál? pomoci. Nicmén? jsme vytvo?ili pr?vodce ?asto kladenými dotazy k náboru. Klikn?te na, kde najdete odpov?di na mnoho otázek, které dostáváme. D?ležité upozorn?nà pro pracovnà agentury GSK nep?ijÃmá doporu?enà od pracovnÃch agentur a/nebo zam?stnaneckých agentur ohledn? volných mÃst zve?ejn?ných na této stránce. VÅ¡echny pracovnà agentury jsou povinny kontaktovat obchodnà a obecné nákupnÃ/lidské zdroje GSK, aby zÃskaly p?edchozà pÃsemné povolenà p?ed doporu?enÃm jakýchkoli kandidát? do GSK. ZÃskánà p?edchozÃho pÃsemného povolenà je podmÃnkou jakékoli dohody (ústnà nebo pÃsemné) mezi pracovnà agenturou a GSK. V p?Ãpad?, že takové pÃsemné povolenà nebude zÃskáno, budou jakékoli kroky provedené pracovnà agenturou považovány za provedené bez souhlasu nebo smluvnà dohody s GSK. GSK proto nebude odpov?dná za žádné poplatky vyplývajÃcà z t?chto krok? nebo za žádné poplatky vyplývajÃcà z jakýchkoli doporu?enà pracovnÃch agentur ohledn? volných mÃst zve?ejn?ných na této stránce. Upozor?ujeme, že pokud jste licencovaný zdravotnický profesionál v USA nebo zdravotnický profesionál, jak je definováno zákony státu, který vydal vaÅ¡i licenci, GSK m?že být povinna zaznamenat a nahlásit výdaje, které GSK vynaložà vaÅ¡Ãm jménem, v p?Ãpad?, že vám bude poskytnut pohovor na zam?stnánÃ. Tento záznam p?ÃsluÅ¡ných p?evod? hodnot je nezbytný k zajiÅ¡t?nà souladu GSK se vÅ¡emi federálnÃmi a státnÃmi požadavky na transparentnost v USA. Pro vÃce informacà navÅ¡tivte webové stránky Centers for Medicare and Medicaid Services (CMS) na https://openpaymentsdata.cms.gov/
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