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.
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
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
Associate Director of Regulatory Affairs is offered on a six month basis and is office based in London. One of the key objectives is to plan/manage/execute regulatory activities relating to global regulatory leadership for one or more projects. Providing regional regulatory therapeutic area strategic guidance on development projects and marketed products.
Senior Regulatory Affairs Associate
New Year, new budget is the mantra for many pharmaceutical companies at the moment! For this reason, a fantastic opportunity has become available with a leading CRO based in Berkshire, for a Senior Regulatory Affairs Associate. This CRO is renowned for its expertise in Clinical Trials and is therefore seeking an experienced Regulatory Affairs professional to join their EU team and work on the compilation and submission of Clinical Trial Applications.
Associate Director Regulatory Policy and Intelligence opportunity has arisen with a leading Research based Biotherapeutics Company in the South East on a permanent basis with an excellent salary and benefits package on offer. This is a highly visible role with regular liaison with internal cross-functional departments and external Regulatory Agencies and associations.
This is great role with enough scope to keep you interested and enough development opportunities to allow you to continue to grow as a regulatory professional. 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
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.
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