Our Client is a leading and worldwide operating biopharmaceutical enterprise whose German subsidiary is based in the greater Munich area in Germany.
Be responsible for the market leading portfolio of drugs for a company that has a great ethic approach and will foster your personal development with strong impulses.
At the beginning you will first of all get to know your portfolio, your team and cross functional partners, the next step is operating your portfolio in regulatory affairs with all needed actions such as Clinical Trial applications, amendments and other clinical trials submissions.
We are searching as soon as possible for a dedicated and experienced
Regulatory Affairs Manager (m/w/d)
Greater Munich area
Art der Anstellung: