Associate Director Regulatory Affairs â€“ lead early stage projects for development in the US, Europe and International â€“ FULL RELOCATION to the Netherlands ... This is a Global Regulatory Lead role graded Associate Director.
Are you a Renior Regulatory Operations Specialist who would now like the opportunity to grow your experience and expertise for a company who will always appreciate, respect and reward your effortsâ€¦??? Join a Department where there is no limit on your own development and where you will be asked to push forward systems and process. Call Theo Moore for full details on this role on +44 207 801 3384
There is an excellent salary available for this role (up to 110,000 Euros) and this position also offers a fully expensed Car, Attractive Bonus, Shares and a Full- Re-location Package. If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380 or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
An excellent opportunity has arisen for a Associate Director to join the European Regulatory Affairs team in a niche pharmaceutical company, who specialise in Orphan Drugs, in Berkshire. As Associate Director, you will be responsible for the implementation of regulatory strategy for selected drug development products and/or marketed products.
We are working in partnership with a fast growing pharmaceutical company based in Berkshire who is looking for a Associate Director in Regulatory Affairs. This is an excellent opportunity for an Associate Director to join the European Regulatory Affairs team in the niche area of in Orphan Drugs.
As a high performing organisation, my client is committed to growing and developing their people and within this International multi-cultural regulatory department you will find challenges and opportunities to keep you interested, motivated and developing for many years to come. If you wish to apply for this role send your CV to email@example.com or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
Within this role you will operate as the EU and ROW regulatory partner reporting into a locally based Global Regulatory leader - If you wish to apply for this role send your CV with a covering note to firstname.lastname@example.org quoting reference number noted above. Alternatively to have a confidential call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380.
Associate Director Regulatory Affairs Emerging Markets opportunity has arisen with a leading Global BioPharmaceutical company on a permanent basis in the South East. My client's Regulatory emerging markets department is rapidly expanding as they continue to develop their exciting portfolio globally.
An opportunity has arisen for an experienced Regulatory Affairs CMC Emerging Markets specialist with a growing Global BioPharmaceutical company with an exciting and varied pipeline of products. You will be responsible for strategically ensuring that the preparation of Regulatory submissions for commercial products in multiple emerging markets according to regional litigation and company policies and procedures.
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