Senior Director for Global Regulatory Affairs
I'm currently hiring for one of my long established clients for a senior director for global regulatory affairs. The role is open as the company have grown significantly over the last few years and ultimately will look to continue this growth in the years to come with many new product launches world wide. What we look for is an experienced regulatory affairs professional with broad pharma regulatory experience across EMA/FDA, post marketing and new launches. The company are still relatively small and will need someone who can be dynamic, hands on and have a commercial mind set.
I've worked with this Pharmaceutical Company for close to 8 years now, so I'm happy to talk through case studies and the pro's and cons. The key take away is it's a good role for someone who wants to be in a smaller, more commercial environment. It's worlds apart from big pharma and there is a lot to learn here that wouldn't necessarily come up in bigger companies. The company are heavily focused on post marketing and product acquisitions, so as such, they are less focused on drug development, hence someone more interested in commercial regulatory would be needed.
If you could be interested 'In-principle' then feel free to contact me. Interest may well be high and the requirements will be very strict, so I will be open with applicants around this.
Reports into: EVP for Regulatory Affairs
For a confidential discussion about this role, or to apply, then send your CV to firstname.lastname@example.org or call me, Matt Beedle, Executive partner on +41 43 50 80 81, ask to be transferred to extension 3290. Please feel free to visit my linked-in profile to see my references/recommendations.
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