Regulatory Program Manager- Pre Approval

Aug 14, 2019
Sep 13, 2019
Matt Beedle
Jobseeker Type
Organization Type
Clinical Practice
Contract Type
Full Time

Regulatory Program Manager- Pre Approval, 6+ month contract, working key pre approval filings for innovative products

Excellent opportunity to work with a top tier pharma company on one of their regulatory development programs. Specifically we search for someone with some experience of pre approval regulatory who is interested in working in the Basel area. I believe the role would be great for someone wanting to get big pharma experience and for anyone passionate about drug development. In addition to this, contracts are often extended and this type of experience in it's self is gold dust when it comes to regulatory development. If you could be interested 'in principle' then feel free to contact me!


  • Broad coverage of regulatory processes for project management
  • Input and help towards CTA, IND and other MA related documents
  • Help with regulatory strategy and planning for scientific advice and HA meetings

Key Requirements:

  • Life science degree
  • 2+ years experience in regulatory affairs for Pharma Rx, ideally some experience in pre approval activities such as INDs, CTAs (especially if you are relocating)
  • Fluency in English

For a confidential discussion about this role, or to apply, then send your CV to or call me, Matt Beedle, Executive partner for Switzerland on +41 43 50 80 817. Please feel free to visit my linked-in profile to see my references/recommendations.

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Luxembourg, Switzerland, Romania, the US and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

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