Senior Regulatory Affairs Consultant

 

Your tasks

  • You are part of our international Regulatory Affairs team and report directly to the business directors
  • As a team leader, you will be supervising Regulatory Affairs Managers and Assistants and ensuring the quality of the project work
  • You coordinate all the necessary activities in the project team, with customers, government representatives and our external partners
  • You expect a variety of projects for the submission of European approval procedures (CP, DCP, MRP), as well as Clinical Trial Applications and activities in the areas of CMC and Post-approval activities, e.g. Promotional Material Reviews

 

Your profile

  • Studies in Pharmacy, Biology or other Sciences
  • Several years of experience in Regulatory Affairs at a pharmaceutical or consulting firm
  • You are distinguished by your leadership skills and your ability to work independently, and also by good communication skills and attention to detail
  • Business fluency in German and English and an adept use of common PC applications (Microsoft Office) complete your profile

 

Our offer

  • Responsible and demanding work in a motivating working environment with appropriate compensation
  • Flexible working hours and the opportunity to optimize your work-life balance
  • Workplace in the attractive University city of Heidelberg

 

Apply with your cover letter and CV at: jobs@eudrac.com