Regulatory Affairs Manager

Cancer Research UK

Stratford, London, GB
Base: £55,000 - £60,000; bonus/equity: not specifi...
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Regulatory advice and support
Clinical trial authorisation applications
Investigational medicinal product dossier
** Cancer Research UK is seeking a Regulatory Affairs Manager to join their Centre for Drug Development in Stratford, London. The role involves providing regulatory guidance for early-phase oncology trials and requires experience in regulatory affairs, particularly related to clinical trials. **

Job Summary

  • We’re looking for an experienced regulatory affairs professional to join our Centre for Drug Development as a Regulatory Affairs Manager.
  • In this role you’ll be providing expert regulatory advice and support to cross-functional project teams within the CDD, supporting the preclinical development and clinical trials of a varied portfolio of novel oncology products.
  • We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools.

Matching Summary

Match Score: 75

** Cancer Research UK is seeking a Regulatory Affairs Manager to join their Centre for Drug Development in Stratford, London. The role involves providing regulatory guidance for early-phase oncology trials and requires experience in regulatory affairs, particularly related to clinical trials. **

Salary

Base: £55,000 - £60,000; Bonus/Equity: Not specified; Benefits: plus benefits

Skills & Requirements

Must-have

  • Regulatory advice and support
  • Clinical Trial Authorisation applications
  • Investigational Medicinal Product Dossier
  • UK and EU regulatory requirements
  • Early phase drug development

Nice-to-have

  • Chemistry, Manufacturing and Controls (CMC)
  • Act with ambition, courage and determination
  • Act with rigour and professionalism
  • Act to have a positive impact on people
  • Act inclusively and collaboratively

Key Requirements

  • Degree in a scientific discipline or equivalent relevant experience
  • Experience of working in regulatory affairs
  • Experience writing and reviewing IMPDs
  • Excellent knowledge of current Clinical Trial Legislation

Work Rights

Must be eligible to work in the UK

Tailored Resume

Cover Letter