Barrington James are exited to post a fantastic opportunity for one of our close clients. This company is a big Pharmaceutical in the UK. They are backed by some serious investors the industry and are looking for future support within their Regulatory Affairs team. This opportunity is prefect for someone who is ambitious, independent and wants to play a key role in working on the most innovative projects.
Key Responsibilities
Lead regional filing strategies for pharmaceutical products across Europe, the Middle East, and Africa (EMEA).
Establish and optimise regulatory structures across the region, managing relationships with key regulatory agencies directly.
Oversee affiliate-level Regulatory Affairs activities across the UK & Ireland cluster, managing approximately 12–13 marketing authorisations in both places
Develop regulatory strategy throughout the product lifecycle, from clinical development through to commercialisation.
Collaborate cross-functionally with internal stakeholders to ensure alignment on regulatory objectives and successful execution of submission plans.
Candidate Requirements
Minimum 8 years of Regulatory Affairs experience within the pharmaceutical industry.
Strong experience supporting drug development programmes from clinical phase through to commercial launch.
Prior experience as an EMEA Regulatory Lead is strongly preferred.
Ophthalmology experience would be advantage, but is not essential.
Background within innovative pharmaceutical organisations such as Alcon, Novartis, AbbVie, or similar is highly desirable.
Fluent in English, both written and spoken.
Proactive, self-motivated, and able to work independently while contributing as a strong collaborative team player.
This truly is an exiting opportunity for someone to join an ambitious company who are continuing to impress the market with their ground-breaking studies.
The opportunity has understandably been incredibly popular. We encourage all interested candidates to apply immediately as it is likely that recruitment will close prematurely.
By clicking “apply” you will be sending your CV to Isobella at Barrington James. Isobella is an RA/QA Recruitment specialist and will discuss the opportunity in detail with you, facilitate your application and will manage the process acting as a link between the company and yourself.
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