Regulatory Affairs Freelancer/Contractor

£27.49 - £70.68 per hour + Negotiable
Jun 19, 2017
Jul 19, 2017
Matt Beedle
Jobseeker Type
Organization Type
Clinical Practice
Contract Type
Full Time

Regulatory Affairs Freelancer/Contractor, Pre-Approval, Long term contract

We are currently looking for an experienced regulatory affairs professional to join a booming development team with many exciting projects from PI-III. Critical to this role will be having someone with experience in CTAs/INDS/IMPD, who understands working with the EMA. The contract can be long term and as such we are open to traditional freelancers, but also candidates who are looking at permanent roles. The reason for this is that NonStop is a licensed labour provider in Switzerland and we can offer payroll options that in essence, offer the benefits of permanent work (Contract, holiday, sickness pay etc). If you are interested in 'principle', then please contact me.

The Clients:

  • A major reason that makes this role exciting is the depth of the pipeline and the long-term options that can become available. There is a high chance this role will move to permanent and can expand into strategic options as well
  • In addition to the pipeline, the company are well established, have many of their own operations and will likely have EU and US expansion plans. With this in mind, it is a good time to join.

Key Requirements:

  • Regulatory pre-approval experience with the EMA in Pharma Rx
  • Life science degree
  • Ability to work in the south of Switzerland for the short to medium term
  • Fluency in English

For a confidential discussion about regulatory affairs, or to apply, then send your CV to or call me, Matt Beedle, Regulatory Affairs Consultant for Switzerland on +41435 080817. For regular job updates and market information please join the Switzerland regulatory affairs linked-in group.

I am a specialist headhunter(recruiter) for regulatory affairs in the Pharmaceutical & Biotechnology industry. I offer a number of search options within the industry with a special focus on the Swiss regulatory affairs market as well as ATMP(Advanced Therapeutics) and biological regulatory professionals worldwide. Please refer to for references.

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