Be a key part of a Queen’s Award winning company

  • Work in a smaller company environment with increased visibility and opportunity to make an impact.
  • Member of the management team to develop and grow the company.
  • Diversified role and exposure to a variety of therapeutic areas and procedures (ODD, PIP, scientific advice, PRIME, centralised MAAs, post authorisation).
  • Opportunity to manage client relationships and be directly involved in regulatory strategy and writing with an emphasis on clinical documents.
  • Part of the UK management team leading development and growth of the company
  • Provides a full range of consulting services to clients to a high quality and on time delivery.
  • Leads project activities.
  • Line management.
  • Is a source of regulatory expertise in the development, registration and post-licensing activities of pharmaceutical products with a focus on clinical activities.
  • Contributes to the effective functioning of EUDRAC.

Location: Chalgrove, OX44 7RW

For more details on requirements and responsibilities, please view the job description online at:

Please apply via email to with your CV and cover letter.