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Senior Regulatory Affairs Director

AstraZenecaCambridge, Cambridgeshire

Salary
£62k – £62k
Posted
12 July 2026
Work mode
Full-time
Sponsor match
high
Skilled WorkerWorker (A rating)
Role overview

AstraZeneca is hiring a Senior Regulatory Affairs Director in Cambridge, a full-time scientific & qa role. The advertised salary is £62k – £62k. AstraZeneca holds an active licence on the UK Home Office register of sponsors for the Skilled Worker route, which means it can sponsor a visa for this hire if it chooses to.

Senior Regulatory Affairs Director Introduction to role: The Senior Regulatory Affairs Director (RAD) leads the development and implementation of global regulatory strategy for one or more products of high complexity and visibility, and may serve as Franchise Global Regulatory Lead (GRL) on complex programmes with multiple indications. Where applicable, this role also operates in a dual capacity, serving as a regional lead based on location, in addition to GRL responsibilities. Central to this …
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AstraZeneca is confirmed on the UK Home Office register of licensed sponsors for the Skilled Worker visa route (Worker (A rating)). Always confirm sponsorship availability for this specific role directly with the employer when you apply.
Visa sponsorship snapshot
  • Employer: AstraZeneca — confirmed licensed sponsor
  • Visa route: Skilled Worker
  • Advertised salary: £62k – £62k
  • How this salary compares: about 52% above the £41,185 median across 546 scientific & qa roles with published salaries on FindSponsorJobs
  • Location: Cambridge, Cambridgeshire · Full-time
  • Similar roles nearby: 14 other live scientific & qa roles in Cambridge browse them
  • Posted: 12 July 2026
  • How we verify sponsors: employers are matched against the UK Home Office register of licensed sponsors — read our methodology.
About this sector

Scientific and quality assurance roles span pharmaceutical, biotech, clinical research, and laboratory sectors. The UK life sciences industry actively recruits internationally for research scientists, QA managers, regulatory affairs specialists, and clinical trial coordinators, with many employers maintaining well-established sponsor licence operations.

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