Job Details

Job Summary:

Expanding biopharmaceutical company in Brussels is recruiting a Senior Manager with experience of pre and post approval projects. You should have the ability to work in a fast paced and change-oriented environment and have experience of taking a project through a registration procedure or late phases of development. Contact Theo Moore now on +44 207 801 3380 for full details on this role.

Requirements:

Brussels based Snr Regulatory Affairs Manager role – EU & US role with Pre & post approval projects

Location: Belgium, Brussels

We have a new Brussels based senior manager of Regulatory Affairs role for an expanding biopharmaceutical which is showing huge potential to be a big success in the next 2-3 years

The role covers:
• Pre & post approval projects
• Centralised filings
• Regulatory Strategy
• HA interaction and Scientific advice meetings
• US regulatory projects

Benefits include:
• Great salary
• High value re-location package
• Private Schooling fees paid
• Growing company with a dynamic working environment

For full details on all Brussels based Regulatory Roles email your CV to Theo Moore or Matt Greig at CV@advregulatory.com or call +44 (0)207 801 3380 

The successful candidate will manage regulatory activities for the on-going registration and post-registration activities in selected markets (EMEA). In addition, the role offers regulatory development activities for a compound in clinical development and US Regulatory exposure.

Experience:
• At least 5 years of experience in regulatory in the pharmaceutical/biotech industry, including regulatory submissions within Europe
• Excellent understanding of post- registration processes (variations) in the EU, including centralised procedure
• Experience in development (CTA, meeting with HAs, development plan, etc...)

This is a dynamic environment for a company with an extensive pipeline. Ideally you will be a highly motivated professional, ready to take the lead for EU and then global Regulatory strategies and submissions.

Excellent salary, bonus, possible car allowance and re-location.
 

Advanced Regulatory have established relationships with the nearly all of the worlds leading Biotechnology, Pharmaceutical, Medical Devices & Clinical Research Consulting companies.

Apply here at Cv@advregulatory.com or go online to see our full selection of roles at www.advregulatory.com - Contact Theo Moore or Matt Greig  on +44 207 801 3380

We work in the strictest of confidence and will NOT submit your CV to ANY client WITHOUT your prior consent, so we are ideally placed to find your next permanent or contract position within Regulatory Affairs.

 

Keyword / Keywords:
Regulatory Affairs / Regulatory Affairs / Regulatory Affairs / Regulatory Affairs / Regulatory Affairs / Regulatory Affairs / Regulatory Affairs / Regulatory Affairs / Regulatory Affairs /
Brussels, Brussels, Brussels/ Regulatory Project Manager / Regulatory Director / Regulatory Manager / Regulatory Executive / Regulatory Officer / Regulatory Operations / CTA / CTA`s / Clinical Trials Application / Centralised procedure / CRP / Clinical / CMC / MRP / Mutual Recognition Procedure / Drug development / Pharmaceutical Development /