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Regulatory Affairs Director Contract - Execution team

Hays • The City, Central London

Salary
£75k – £75k
Posted
16 September 2026
Sponsor match
high
Skilled WorkerWorker (A rating)
Role overview

Hays is hiring a Regulatory Affairs Director Contract - Execution team in The City, a scientific & qa role advertised as contract. The advertised salary is £75k – £75k. Hays 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.

12-Month Contract | Hybrid Working | Potential to Convert Permanent About the Role I am supporting an Oncology biotechnology organisation seeking an experienced Regulatory Affairs leader to oversee the execution of global regulatory activities across a clinical-stage portfolio. This role requires a strong people leader with proven experience delivering US and EU regulatory submissions, leading regulatory teams, and ensuring successful execution of regulatory strategies across multiple developme…
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Hays 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: Hays — confirmed licensed sponsor
  • Visa route: Skilled Worker
  • Advertised salary: £75k – £75k
  • How this salary compares: about 85% above the £40,524 median across 946 scientific & qa roles with published salaries on FindSponsorJobs
  • Location: The City, Central London
  • Similar roles nearby: 5 other live scientific & qa roles in The City — browse them
  • Posted: 16 September 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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