- PW 6283 Director/Senior Director Regulatory Affairs
This is a key opportunity for an experienced regulatory professional to play a Deputy Head role with broad responsibility for the Neuro and General Medicines therapy area of this global Pharma company. You will hold budgetary responsibility, attend key EU Health Authority meetings, play the EU regulatory lead for key General Medicines development projects and closely monitor the regulatory environment.
- Regulatory Affairs Associate Director – Brussels - Take the lead for Centralised filings and EU/ROW strategy – Salary to 120,000 + Car + Bonus
As a high performing organisation, my client is committed to growing and developing their people and within this International multi-cultural regulatory department you will find challenges and opportunities to keep you interested, motivated and developing for many years to come.If you wish to apply for this role send your CV to email@example.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380
- Regulatory Affairs Manager - South East - Expanding Biotech in the M4 Corridor with an excellent pipeline for Oncology and Immunology
There are options available to work on Products in Phase I, II & III through to MAA for both Pharma and biotech (Monoclonal) products. If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380
- Regulatory Operations Lead
Regulatory Operations Lead EU - Global Pharma Business
Hertfordshire / North London, UK
Salary: £60,000 - £70,000 per annum
- Deputy Head of Regulatory Affairs - Neuroscience and GM
Senior Director, Regulatory AffairsAn extremely successful midsize pharma company based on the outskirts of North London are looking to recruit a Senior Director Regulatory Affairs to be the Deputy Head for their Neuroscience and General medicine department to join on a permanent basis. ...
- Regulatory Affairs Manager - Established Products
A fantastic and immediate need has arisen at a global pharmaceutical company for a Regulatory Affairs Manager to join the team. You will be responsible for Established Products within your designated therapeutic area (CVM) My client is a research-based global pharmaceutical company, and is amongst the leading pharmaceutical companies in the world.
- MAINLAND EUROPE *** Global Therapy Regulatory Lead ** Lead the leaders role, stakeholder facing … Great LT and package
This role is available to US candidates willing to work globally, as well as Swiss and EU Citizens. The company will provide you and your family a full relocation package including schooling, tax support and Visa. Working globally greatly enhances your prospects so consider my opportunity as a ladder to the top. For US callers, dial 011442078013380 ... or email us today ... to CV@advregulatory.com
- Regulatory affairs Manager
My client who is a new start up consumer focussed organisation are currently recruiting for an EU Regulatory Manager. They are based in Central London and looking for somebody who has a deep knowledge of Regulatory Affairs working with Consumer Healthcare products. ...
- EU and Global Regulatory Development & MAA roles –Based in the UK, Switzerland, Belgium or The Netherlands – From Advanced
Please have a read and let me know if any of these roles are of interest. If there another type of role in another location that would be more interesting/suitable for you, then please let us know as we work some of the world’s leading Pharmaceutical and Biotechnology companies based all over Europe If you wish to apply for this role send your CV to email@example.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380 -
- Associate Director Regulatory Afffairs - Contract Job
Purpose• Demonstrably the affiliate expert in quality and regulatory, acting as the primary point of contact for all affiliate quality and regulatory issues. ...