The company view this role as a Director position but are open on grading if required either way. The company are offering a red carpet relocation - To apply contact Theo Moore or Matt Greig, in the UK London office, via CV@Advregulatory.com or call +44 (0)207 801 3380 0r +44 (0)7918 679 405 (eves / weekends)
You will be joining a leading provider of pharmaceutical support services as a Senior Regulatory Associate. This company partners with life science companies to make medicinal products safer and more accessible for the consumer and through acquisitions; our client has grown from strength to strength. They handle both clinical and post approval work, however their speciality is clinical. Previous regulatory experience within a CRO is required and you will need a minimum of 2 years.
This company is highly rated within the industry and is well on itâ€™s way to becoming the worlds No.1 Pharmaceutical Company. The pipeline is rich and diverse, and includes Pharma and Biotech compounds. For this role you will operate as the EU Regulatory liaison for Oncology. 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 London office on +44 (0)207 801 3380 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
A dynamic, expanding and leading Switzerland based Global Pharma company is looking for someone special. They seek a regulatory affairs Assoc. Director with experience of Major project management for EU and Global projects with in-depth knowledge of PIP's, EU Stratergy and MAA submissions. The next step will be Diretcor with team leading responsibilities. Call Theo Moore or Matt Greig on +44 (0)207 801 3384 for full details or to apply for this role send your CV to Theo@advregulatory.com
You will receive excellent promotion prospects and those who achieve good levels of success in EU submissions will quickly be promoted into a Global position. 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
EU Regulatory Affairs Manager / Regulatory Affairs Manager - Clinical Trials
Up to ÂŁ60,000 per annum plus benefits
As the successful EU Regulatory Affairs Manager you will be joining our client who is a leading provider of pharmaceutical support services, partnering with life science companies to make medicinal products safer and more accessible for the consumer.
You will be working both with technical operations and manufacturing sub committees as well as with the global regulatory leaders for your assigned projects, to define strategy for CMC as well as provide input / decision making both to the GRL's - Contact Theo Moore or Matt Greig, in the UK London office, to CV@Advregulatory.com or call +44 (0)207 801 3380 or +44 (0)7918 679 405 (eves / weekends)
My client is a highly successful and expanding a Bio-Pharmaceutical company with an extensive pipeline and a high value commercial portfolio who is seeking a dynamic, innovative and highly motivated personality to take the lead for EU (and sometimes Global) Regulatory strategies and submissions. This role comes with an excellent salary; fullâ€“relocation package & excellent career prospects. Contact Theo Moore on +44 (0) 207 801 3384
If you feel this appeals to you, then please apply to Matt Greig, at Advanced Search & Selection on +44 (0)207 801 3382 (or +44 (0)7918 679 405 after hours). Alternatively drop me an email with a full CV to firstname.lastname@example.org in confidence
Just Pharma are assisting a leading global company in their search for a Regulatory Manager to lead their EU regulatory team, to be based in the office in London.
The client is offering a very competitive salary and benefits package as well as further opportunities for career growth.
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