- Regulatory Affairs Director / The Netherlands / EU and then global leadership of development and filing strategies
My International pharmaceutical client is looking for a talented regulatory affairs Associate Director to provide strategic & operational support to Global & regional based project teams for both development & Life-cycle management projects. You will also have at least 10 years experience of hands on European regulatory activities in a matrix environment and be looking for a highly visible position. Contact Theo Moore or Matt Greig on +44 (0) 207 801 3384 or email CV@advregulatory.com
- Regulatory Affairs Director / EU & Global regulatory strategies - line management and project management role / Brussels
This exciting Biotechnology client based in Brussels is looking for someone special. They seek a regulatory affairs Director with experience of both line management and project management for EU and Global projects with In-depth knowledge of Paediatric Investigation Plans and Orphan Drug Designation applications. Call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
- Regulatory Affairs Manager, CMC Biologicals - EU Liaison role - Receiving training to become a GRL
If you wish to apply for this role, please send your CV with a covering note to email@example.com or alternatively, to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
- Regulatory Affairs Associate Director*** The Netherlands*** Manage regulatory teams through all aspects of product development***
My Blue chip Pharmaceutical client is looking for a Regulatory Leader who is happy and confident to lead the submission and approval of a Marketing Authorisation Application for a new active substance, line extensions, major MAA variations, definition of the EU regulatory strategy and all major agency interaction. Excellent salary, good bonus, generous car allowance and full benefits and re-location package available. Contact Theo Moore or Matt Greig on +44 (0)207 801 3384
- Regulatory Affairs Associate Director - Netherlands - EU & International strategic leadership role - Excellent Portfolio - Expanding Pharma Company
By joining this amazing organisation you will follow a large numbers of employees who have built unique and rewarding careers as the company has grown. With continued growth on the horizon, there's no end in sight to your career possibilities! This will be a results orientated strategic leadership role where your strategy and regulatory knowledge will carve a path for product submissions and registrations. Call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
- Regulatory Affairs Director EMEA - Lead the development strategy and L/Cycle management for Oncology indications - Amsterdam or Leiden
Operate as the Regulatory lead for a Global Brand in Oncology - Lead the development and Implementations of regulatory strategies for MAA’s within the EMEA region - Identify future commercialisation opportunities for worldwide markets. To apply for this role, please send your CV with a covering note to firstname.lastname@example.org or alternatively, to have a confidential discussion about this or other potential roles call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
- Senior Regulatory Affairs Manager - OTC
Do you have a strong eye for detail coupled with an analytical mind, with experience in the pharmaceutical industry and Regulatory Affairs? You might be just what we're looking for…Your previous experience in the pharmaceutical industry will help you in supporting the OTC RA team in with pre-market RA activities from assessment, strategies, compilation, submission, outcome delivery and overall guidance for OTC medicinal products.
- International RA Strategy Lead
A global, highly specialised Biopharmaceutical company based in Switzerland are growing in size. They have reorganised their Regulatory Affairs division to accommodate a growth in business and product portfolio. New positions have been created in two therapy areas - Neuroscience and Genetic Disease. Your job title in this position will be International Strategy Product Lead and you will report into the Head of the group directly.
- Regulatory Affairs Director of CMC – Brussels – Global role with Team Leading
My client is offering a strong salary at the upper end of the pay scale with a number of strong benefits/initiatives around full re-location, private healthcare, stock options, sign on allowances, housing allowances , fully expensed company car with petrol card, bonus & school fees paid for one of the International Private schools in Brussels. Call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380
- IMMUNOLOGY Senior Medical Development Lead *** Lead Ph2A/B & Ph 3 *** Based US or Europe
My client is developing new medicines (mostly biologicals) and new line extension new indications, and is spending around 20% of their T/O on R&D, as they are pushing in to new disease segments altogether from their vantage point of RA in to Dermatology.