Company: Advanced Regulatory (UK & Europe)
Location: Brussels, Belgium
Reference: TMADV / 111016B
Closing Date: 11 Nov 16
Type: Full Time
Salary (£): On Application
Benefits: On Application
As the EMEA Regulatory Team Lead you will play a pivotal role in providing support to the GRL with respect to mentoring & leading the team for all types of submissions and strategic initiatives. If you wish to apply for this role please click below, or send your CV with a covering note to email@example.com quoting reference number noted above or call Theo Moore or Matt Greig on +44 207 801 3380
Regulatory Affairs EMEA Team Leader – Join a growing biotech in a Strategic RA role for EMEA MAA activities
Location: Belgium, Brussels
Take responsibility for a number of key projects in this high level strategic role which will include providing input into the Global Regulatory Liaison for development strategy, submitting Clinical Trial Applications, project managing submission of Scientific Advice briefing packages & MAAs(or line extensions/Type II variations) for an expanding biotech company that has shown great levels of growth in the last 3 years.
As the EMEA Regulatory Team Lead you will play a pivotal role in providing support to the GRL with respect to mentoring & leading the team for all types of submissions and strategic initiatives. You will be responsible for leading strategic decisions on development projects through the Centralized procedure MAA’s (as the agency liaison) as this department continues to take the lead for high profile success filings.
The salary for this position is up excellent with a performance related bonus of approx. 20% bonus, fully expensed car, highly lucrative share scheme and extensive relocation package which includes removals, storage and unpacking of items, a settling in-allowance and company apartment for up to 6 months
The holder of this position would take responsibility for a number of key projects for which they will co-ordinate all EMEA regulatory activities whilst leading a team of strong and motivated regulatory performers. For development projects, this would include providing input into the Global Regulatory Liaison for development strategy, submitting Clinical Trial Applications, project managing submission of Scientific Advice briefing packages, MAAs (or line extensions/Type II variations). For maintenance activities, this would include the compilation of regulatory strategies, coordinating any submissions via collaboration with local Regulatory contacts, liaising with Commercial and mentoring/supporting junior team members.
If you wish 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 or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Advanced Regulatory is a division of Advanced Search and Selection Ltd and has been operating since 2004. We are registered and licensed to recruit through the United Kingdom, mainland Europe and the Americas - we have offices both in the UK and in Switzerland. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory Affairs.
We match professional candidates to the best permanent, contract and interim roles in the market. For more information about the company visit us at www.advregulatory.com.
We provide a high level of service because we believe this matters. Regulatory professionals will find we know our recruitment subject matter.
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