Associate Director, Regulatory Affairs

£108275.70 - £141591.30 per annum + Negotiable
Sep 26, 2020
Oct 26, 2020
Matt Beedle
Jobseeker Type
Organization Type
Clinical Practice
Contract Type
Full Time

Associate Director, Regulatory Affairs, Pre Approval, Geneva Region

Excellent opportunity to be a part of the regulatory development of a range of innovative pharma and biotech products. The company have a significant pipeline of products in very targeted TA areas and are looking to further expand this. The responsibilities in this role will be both strategic and operational and will cover aspects from scientific advice, INDs, PIPs, CTAs all running towards MAA submissions.

If you are passionate about science as well as regulatory affairs, then this role is one to seriously consider. If you could be interested 'in principle' then feel free to contact me.

Key Responsibilities:
* Helping across many regulatory processes for the EU and some FDA pre approval including CTAs, PIPs and scientific advice
* Helping to work with vendors and commercial partners
* Coverage for both hands on submissions and strategic input

Key Requirements:
* Over 6 years experience in regulatory affairs for pharma
* Proven experience in pre approval regulatory affairs in pharma (Such as scientific advice, a leading role in a new MAA process)
* Life science degree
* Fluency in English

Open to relocators? Yes, we can consider candidates who are EU citizens. French is nice to have, but not a pre requisite.

For a confidential discussion about this role, or to apply, then send your CV to or call me, Matt Beedle, Associate partner for Switzerland on +41435 080817. Please feel free to visit my linked-in profile to see my references/recommendations.

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