OPTION SUISSE ** EU Regulatory Liaisons & Strategy Leaders ** Great Package, Car, Bonus & Stock, Relo Available!

Reference: JM060522

Expiry Date: 01-09-2022

Categories Biotech, Regulatory Affairs

Salary: On Application

Job Type: Full Time


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Job Description

Switzerland offers one of the best lifestyles and environments to work in!

We live in exciting times so my team and I are pleased to offer positions at Associate Director and Director grade, in European Regulatory Affairs, with a focus on late development and registration or major brand lifecycle (we have multiple vacancies).

The positions are for individuals 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, they support the coordination) and an investment in R&D in excess of 14 Billion USD annually.

  • These roles are in Switzerland but not in Basel, relocations are offered within CH and within the EU to this location, it is a well-funded relocation
  • These roles come with an extra special salary and benefits package, subsidized healthcare, car or car allowance, as well as stock RSUs and bonus
  • The company is a larger mid-sized company, well known for its reputation, and they are supporting several therapy areas, with class leaders in many of these
  • The company has no me too drugs in development, they are innovators in certain modalities, and have mAbs, NCEs as well as Cell and Gene Therapies
  • We repeat this organization is not in Basel, but is it commutable from certain southern Cantons or from Berne.
  • We have been appointed by the client to source these roles over summer, and we look forward to helping you.

We have two main options for these positions, based in different therapy areas:-

Option A: initial MAA preparation & New Indications filing role: you will be the EU Lead on a late phase molecule in Immunology and lead the molecule to filing in the coming 2 years, the readout has not yet happened; we are looking for an individual who wants a MA Approval on their CV. The P2B data was startlingly good, with very low safety events observed and high efficacy. You will work closely with Global to lead the filing into the EMA, and through for the first round of the New Indications; this role is not for the faint hearted, you will want this because that’s what regulatory ultimately do, gain approvals, and you will know that this builds your career.

Option B: Big brand lifecycle management, you will be an experienced lifecycle regulatory leader who knows how to work with commercial and medical affairs, you will lead the last major indication for paediatrics, and pivot to a new IMP / NBE as the workload draws down. There is an opportunity in this role to move into team leading.

The roles are open to anyone who is from the EU, is willing to Live, Work and Ski in Switzerland, and for individuals who are seeking a long-term career platform.


To Apply!

To apply for this role, please contact me, Christian or my colleague Javier Monfort on Swiss number +41 41 562 01 51 or press the red “Apply for position” button, or send a full CV to cv@advtalent.com. We will support you throughout the interview and on-boarding experience.

GDPR & Data Protection: Your information is safeguarded for GDPR, and you will have the right to edit, amend or delete and ’’be forgotten’’ at any time after your initial registration.