My client is an established consultancy with a focus on innovative early to late phase development projects. They are currently partnered with a large number of the top 20 Pharma and Biotech companies across the world.
This is a fantastic opportunity for the candidate to join this company at a time of expansion. You will lead your own development projects and engage and create new clients worldwide.
-Be the Regulatory lead on early to late-stage product development
-Preparation of regulatory submission documents including orphan drug designation applications
-Assist and lead global health authority interactions
-Provide support for ongoing projects and mentor new staff
The ideal candidate
-The ideal candidate will have around 4 years experience within Regulatory Affairs, ideally within a consultancy environment
-Existing experience with development projects with the EMA and/ or FDA
-Knowledge and experience of ATMP/ Biologics or Small molecules
-Ambition to develop within a growing consultancy
If this position is of interest to you, or you would like to recommend a contact then please get in touch!