Senior Regulatory Affairs Manager, Pre-Clinical, Biologics
Senior Regulatory Affairs Manager, Pre-Clinical, Biologics, EU/FDA, Growing Pharmaceutical Company, Established marketed products as well as new portfolio.
Excellent opportunity to join a brand new program in Biologics development for a well established Pharmaceutical company in Basel. The key to this role will be leading proceedings for IND filings while also having input towards other pre-clinical parts of the portfolio. The role will have broad coverage of pre-IND aspects from CMC to prep books for the FDA and EMA. In addition to this, it will hold an important strategic focus for planning and be working with multiple teams internally. This really is one of these rare RA roles where you can be involved from start-finish. If you are interested in Biologics and the chance to be a part of a brand new portfolio, then please contact me.
- Over 6 years experience in regulatory affairs in pre-approval for Rx products
- Experience in Biologics
- Fluency in English
- Life Science degree
For a confidential discussion about regulatory affairs, or to apply, then send your CV to firstname.lastname@example.org or call me, Matt Beedle, Regulatory Affairs Consultant for Switzerland on +41 43 50 80 817 . Please feel free to check my linked-in account for my references.
For regular job updates and market information please join the Switzerland regulatory affairs linked-in group. https://www.linkedin.com/groups/4550988
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