Expiry Date: 07-02-2023
Categories Biotech, Regulatory Affairs
Salary: On Application
Job Type: Full Time
My team and I are excited to introduce you to this position at Associate Director level, in European Regulatory Affairs, with a focus on late phase development and registration for immunology and cardiovascular programs. The position is for an individual who would like to have ownership of their own programs, backed up by a well-honed organization, the support of regulatory project managers (you own the strategy, and they support the coordination) and an investment in R&D that exceeds 14bn USD annually.
What I like about this opportunity:
As an Associate Director and EU Regulatory Liaison, you will support the initial MAA preparation and New Indications filings. You will be the EU Lead on a late phase molecule in Immunology and/or Cardiovascular and lead the molecules to filing in the coming 2 years, the readout has not yet happened but the Phase 2b data was good, with high efficacy and low safety events.
You will work close with Global to co-lead the filing into the EMA and through for the first round of New Indications! The role is open to anyone who is from the EU and is willing to Live, Work and Ski in Switzerland and for individuals who are already living in Switzerland and seeking for a long-term career platform.
To apply for this role, please contact me Christian Atanasov on +41 41 562 0957 or press the red “Apply for position” button or send me an email to firstname.lastname@example.org and I will reply by return. I will support you throughout the interview and on-boarding experience.
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