Expiry Date: 28-12-2019
Category Regulatory Affairs
Salary: On Application
Job Type: Full Time
***Regulatory Affairs EU Project Manager ***Full project lifecycle role*** Great Training Available!
Location: Brussels, Belgium
This is a great opportunity to be part of something special… and this is the perfect role for a regulatory professional with experience of development projects or supporting MAA’s and/or lifecycle activities to take a central role with a high level of strategic input for EU development projects and CeP submissions for Biological indications in both mid and late stage development.
In the short term you will operate as the strategic regulatory liaison for your projects, and in the longer term you will continue to grow and development experience across a strong portfolio where you will move up to become a Global Regulatory Leader or potentially manage a team.
Within this dynamic global regulatory affairs environment you will be working in a mixed role covering drug development, product registrations & line extensions of biotech products/projects where you will also receive great training and the opportunity to cross into new therapy areas and cover all stages of development.
Excellent training and development opportunities are available, but it essential for you to have some experience of working on regulatory development projects.
To apply for this role, please press the red “Apply for position” button, or contact Theo Moore or Matt Greig TODAY on +44 (0)207 801 3380 for an initial discussion about the role and other projects.
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