Regulatory Affairs Specialist (m/w/d) - Teilzeit

Ort: Bonn, Nordrhein-Westfalen, Deutschland
Gehalt: a. A.
Spezialisierungen: Life Sciences
Vertragsart: Festanstellung
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Regulatory Affairs Specialist (m/w/d)

This position is to be filled part-time.

This tasks are awaiting you:

  • Preparing ethics committee and regulatory submission packages according to relevant polish regulatory requirements;
  • Collecting and updating information on EC and regulatory requirements;
  • Filling, tracking, preparing and maintaining trial documentation
  • Carrying out these duties, you will be fostering close contact with sponsors and site investigators

What you need to get started:

  • Minimum of two years of experience in the clinical trials regulatory field, with a good grasp of regulatory guidelines of clinical trials conduct in Germany
  • Very good organizational skills and attention to details
  • Ability to work to tight deadlines and to prioritise workload in a fast-moving environment
  • Excellent interpersonal skills and strong client service mentality
  • Self-motivated and proactive, with ability to work across multinational teams
  • Good oral and written communication skills in English and German
  • Demonstrable ability to analyse and evaluate complex information
  • Degree in life science or business

Your contact person for this position is Frau Franziska Mayr

You can reach her directly at:

T: +49 (0)89 5519 7774

M: f.mayr(at)

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