A Clinical Trial Regulatory Coordinator with substantial pharmaceutical regulatory affairs experience is required by a leading pharmaceutical R&D company based in the High Wycombe area The ideal candidate will be responsible for leadership of CTAs throughout product lifecycle, as well as development of CT ...
My innovative and expanding medium sized Pharmaceutical client is seeking a regulatory professional with 7+ years broad experience in regulatory affairs covering both pre and post marketing phases of development for a range of therapeutic categories and dosage forms. 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
As your experience grows, so will your level and depth of project responsibility, ultimately leading to you becoming a Global regulatory leader with responsibility for your project in all major regions (EU/US/Asia/LatAm). 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
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 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
An expanding Bio-pharmaceutical company in the Berks/Bucks border is seeking a dynamic personality, with fantastic coms and relationship building skills for Regulatory Affairs Snr EU Manager role where you will lead Product Lifecycle Mgt activities for a Biological portfolio. Contact Theo Moore on 0207 801 3384 or email me in confidence via theo@advregulatory.com
Please call one of Advanced's principals for Regulatory Affairs, Matt Greig or Theo Moore on +44 (0)207 801 3382 or +44 (0)7918 679 405. Alternatively you can email us directly on CV@AdvRegulatory.com
Learn how to provide leadership for regulatory submissions whilst providing strategic and innovative thinking for major pharms and biotech projects/submissions (for EU and/or International territories) - 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
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
Operate as a Regulatory Affairs Manager in role which is based around providing strategic leadership for MAA’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 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
This role comes with direct reports, a car allowance and a very competitive salary. The project work is CMC focused but varied and covers development and marketed products. 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