Join a first class organization that has both Pharma and Biotech products in development, Lead EU Strategy for Biotech submissions & Gain Global regulatory experience -
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 -
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 firstname.lastname@example.org
My blue chip Pharmaceutical client is now looking to expand their EMEA Regulatory affairs team and are now searching for a number of experienced, motivated and talented individuals for a number of Regulatory roles based at their European Head office. Contact Theo Moore on +44 207 801 3380
Operate as a Regulatory Affairs Manager in role which is based around providing strategic leadership for MAAâ€™s, lifecycle and development for products in the EMEA region for Oncology Biotech projects - 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
Join a world leading Pharmaceutical company where you work closely with headquarters to develop global regulatory strategies incorporating EU requirements for assigned projects. Identify risks and develop mitigation plans. 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
Advanced regulatory have a number of new and exciting regulatory affairs roles for an expanding Biotech. My client is looking for a number of forward thinking regulatory affairs Managers who would like to lead EU development projects or provide Regulatory strategy for MAAâ€™s across the EMEA regions.
Contact Theo Moore or Matt Greig on 0207 801 3384 or send your cv to CV@advregulatory.com
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
This role will give you the opportunity to cover stages of development and take the lead for an EU MAA via the centralized procedure in a leadership role where you will be involved in both developing and delivering EU and sometimes global regulatory strategies. Contact Theo Moore on +44 207 801 3380 or email your cv in confidence to Cv@advregulatory.com
Our client, a world class pharmaceutical company driven by research and development, strives towards better health for individuals by developing safe, effective and innovative pharmaceutical products and now ranks as the fastest-growing among the UK's top 50 pharmaceutical companies. They are seeking a Senior Regulatory Affairs Manager for their London location.
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her