This is an exciting time to join a Top Ten Blue-chip Global Bio-pharmaceutical company in a snr level role where you will manage development projects & EU MAA’s via the Centralised procedure for NCE and NBE’s. 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
It’s the variety of the pipeline here that really makes the difference and you will be well matched with a product that suits your expertise - If you wish to apply for this role send your CV to cv@advregulatory.com 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
Take senior level responsibility for liaising with partners in order to facilitate the global regulatory submissions with the Health authorities and operate as a part of a small global Regulatory Affairs team providing regulatory support to operational departments - If you wish to apply for this role send your CV to cv@advregulatory.com 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
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.
This Global Pharmaceutical client is looking for a Regulatory affairs CMC Associate Director to operate as the EU CMC product lead supporting regulatory activities for various NMES and marketed products for a variety of projects. 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
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.
Senior Manager Global Regulatory Affairs CMC opportunity available on a permanent basis in Cambridge, my client is a leading Global BioPharmaceutical company with a great reputation in the market place for their innovative and ethical approach; they are also offering an excellent salary and benefits package for this highly innovative and visible role in their Global Regulatory Affairs CMC team.
Senior Manager Global Regulatory Affairs CMC opportunity available on a permanent basis in Cambridge, my client is a leading Global BioPharmaceutical company with a great reputation in the market place for their innovative and ethical approach; they are also offering an excellent salary and benefits package for this highly innovative and visible role in their Global Regulatory Affairs CMC team.
A Global Study Manager required by global CRO. You'll be working with a recognised global leader in the sector and will enjoy excellent ongoing career developmet opportunities to work towards Associate Project Director level. You must have full-service global Project Management experience gained within a CRO environment. Locations for this role include: UK, Spain, Germany, Italy, Belgium , Netherlands, France, Poland , Romania , Hungary and Czech Republic