clinical research

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Experienced Regulatory Affair Specialist in regulatory affairs and clinical trials for our office in Germany

We are currently looking to recruit a Regulatory Affairs Specialist (RAS) with experience in clinical trials to join our polish operations based in our Bonn office.

As a Regulatory Affairs Specialist, you will have at least two years of experience in the regulatory field of clinical trials and be responsible for the following:


In carrying out these duties, you will be fostering close contact with sponsors and site investigators.

As a successful candidate, you will possess the following core competencies:


We offer you an attractive remuneration package and the opportunity for personal and professional growth in an international environment. If you are a motivated self-starter, and working in a dynamic and growing research and medical consultancy appeals to you, we would like to hear from you.

Please send your application to the following address:

monipol GmbH
Dr. Jaroslaw Stepien
Heilsbachstr 22-24 53123 Bonn Germany
e-mail:; Tel.: +49 228 22787812