In the short-term you will take the lead for EU submissions for NME’s taking responsibility for strategy and major operational activities, before growing into a director level regulatory professional. If you wish to apply for this role send your CV to cv@advregulatory.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
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; full–relocation package & excellent career prospects. Contact Theo Moore on +44 (0) 207 801 3384
This role will give you full hands on Centralised procedure submissions experience then allow you to move into a global role. This really is an excellent opportunity to develop your expertise in a friendly & commercially focused environment for one of the worlds fastest growing Pharma companies.
This is a regulatory role for those who want to influence their own development, who are looking for a position of leadership where you have the opportunity to pursue your interests across functions and geographies.
To contact me email me Theo@advregulatory.com or call me on +44(0)207 801 3384
Join this world’s leading pharmaceutical company and operate in a EU CMC role for Pharma and Biotech products in all stages of development. This role will suit a snr regulatory professional who wants to work on development projects and then move into a Global role.
Lead and provide regulatory strategy to submit scientific advice, achieve the successful application of a PIP and submit and validate an EU centralised MAA. Contact Theo Moore on +44 207 801 3380 or email me in confidence on cv@advregulatory.com
There are currently opportunities to work on products in all stages of development (phases 1,2 and 3) for small and large molecule products in roles that encourage regulatory y leadership, RA strategy, agency negotiation and leading Centralised MAA’s. Contact Theo Moore on +44 207 801 3380 or email me your CV via CV@advregulatory.com
A global pharmaceutical organisation requires a Regulatory Affairs consultant at Strategist-level to join their team and work on a project which involves filing changes for multiple regions. The role is for an initial period of 8 months, based in Basel.
Keywords: Basel, reg affs, reg affairs, regulatory, RA, Regulatory Strategist, Regulatory consultant, Regulatory Executive, Regulatory manager.
With a focus on natural, long-term growth, this Blue-Chip organisation depends on the contributions of talented and committed professionals like you who are determined to drive through progress. In turn, they will make sure your work environment leaves you the space you need to attend to your personal goals, meet your family obligations, and pursue your professional development. Contact Theo Moore for more details on 0044 207 801 3380
This organisation has a healthy pipeline of early and late stage development projects and the regulatory department is uniquely set-up in such a way that you will have full project responsibility and leadership for your own Centralised registrations. If you wish to apply for this role send your CV to cv@advregulatory.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
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