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Global Clinical Program Lead

AstraZeneca • Cambridge, Cambridgeshire

Salary
£59k – £59k
Posted
27 September 2026
Work mode
Full-time
Sponsor match
high
Skilled WorkerWorker (A rating)
Role overview

AstraZeneca is hiring a Global Clinical Program Lead in Cambridge, a full-time scientific & qa role. The advertised salary is £59k – £59k. 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.

Make a more meaningful contribution. Impact patients’ lives every day. Make a more meaningful impact in your career, with greater ownership and accountability to make a contribution. We are looking for people driven by making a difference to patients’ and society, dedicated to doing the right thing. Do you have expertise in Respiratory clinical development and passion for developing late phase clinical program strategies? Contribute to our growing pipeline. Join a place with the commitment, kno…
Before you apply

Applying for this sponsor role?

Get your CV, cover letter, or full sponsor-job application pack prepared before you apply — or let our dedicated application team apply for suitable roles on your behalf.

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: £59k – £59k
  • How this salary compares: about 43% above the £40,932 median across 1,086 scientific & qa roles with published salaries on FindSponsorJobs
  • Location: Cambridge, Cambridgeshire · Full-time
  • Similar roles nearby: 52 other live scientific & qa roles in Cambridge — browse them
  • Posted: 27 September 2026
  • How we verify sponsors: employers are matched against the UK Home Office register of licensed sponsors — read our methodology.

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