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

Reference: SMJ524

Expiry Date: 24-01-2023

Categories Biotech, Regulatory Affairs

Salary: On Application

Job Type: Full Time


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Job Description

We live in exciting times so my team and I are pleased to offer positions at Director level, 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.

Why would you consider these opportunities:

  • These roles are in Switzerland but not in Basel, relocations are offered within CH and within the EU to this location and 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 have many 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 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 Phase 2B data was startlingly good, with very low adverse 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 feint 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 and is willing to Live, Work and Ski in Switzerland, and for individuals who are already living in Switzerland and seeking a long-term career platform.


To Apply!

To apply for this role, please contact Javier Monfort on +41 41 562 0151 or my colleague Matt Greig on +44 207 801 3386 or press the red “Apply for position” button or send us an email to and we will reply by return. 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.