Be part of our Queen's Award winning team
EUDRAC provides regulatory and pharmacovigilance support to drive products through clinical development, registration and life-cycle support in the EU countries.  Our clients range from large multinational companies to small start-ups in Europe and USA.

We need someone with:

  • Enthusiasm
  • Good initiative
  • An ability to engage with existing and future clients
  • Significant regulatory affairs experience including a successful track record in the development, registration and life-cycle maintenance of medicinal products within Europe, particularly in the clinical arena.

Job Description
Client Activities

• Provides a full range of consulting services (strategy and writing) particularly with an emphasis on clinical documents
 (overviews, briefing packages, orphan drug designations, paediatric investigation plans)
• Delivers complex projects on time and to a high quality. 
• Acts as EUDRAC team-lead. 
• Supervises and reviews work of personnel. 
• Interacts professionally at multiple levels within a client organisation. 
• Prepares and/or delivers presentations with minimal support of Management. 

Knowledge Management
• Acts to develop and maintain regulatory skills and knowledge necessary to ensure effective support to clients. 

Business Development
• Continues to build a network of industry colleagues. 
• Assists Management in the preparation of proposals (e.g. researching new potential projects, determining activities required). 
• Manage specified client relationships. 

EUDRAC Activities
• Develops and maintains personal contacts with regulatory agencies or professional associations to build confidence in and enhance the reputation of EUDRAC. 
• Line management.

For further information or to apply, email (no recruitment agencies).