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Job Details

Regulatory Affairs – EMEA Project Manager – A role which covers EU development to registration(s)

Company: Advanced Regulatory (UK & Europe)
Location: South-East
Reference: TMADV / 311017C
Closing Date: 30 Nov 17
Type: Full Time
Salary (£): On Application
Benefits: On Application

Job Summary:

Provide EU and then global regulatory strategy guidance for NME’s in development and through registration & lead Health authority interactions and including Scientific advice through the development lifecycle of your projects - If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.

Requirements:

Regulatory Affairs – EMEA Project Manager – A role which covers EU development to registration(s)

Location: South-East

This is a great opportunity to join one of the world’s fastest growing Biotech’s in a global strategic registrations role. This organization is widely recognized as a great place to work and you will be encouraged to be a high performer, to take real initiative in strategy development and to see things from many angles. You will be expected to handle responsibility with passion, integrity and courage, and be motivated and encouraged to perform at your highest level. The workforce here are high achievers and strive to be successful, grow and develop within regulatory affairs.

In the short-term you will take the lead for EU submissions for NME’s taking responsibility for strategy and major operational activities, before growing into a director level regulatory professional who is highly placed to work through all stages of the lifecycle for development and Global submission strategies.

The role:

  • Provide EU and then global regulatory strategy guidance for NME’s in development and through registration
  • Lead Health authority interactions and including Scientific advice through the development lifecycle of your projects
  • Lead in the preparation / submission of Phase 2/3 CTAs, Scientific Advice/pre-submission meetings and Line Extensions submissions (New Indications / Dosage Forms)

The Package:

  • The salary for this role is exceptional and you will receive a strong bonus plus pension and  healthcare package that covers your entire family – Re-location is also included if necessary

Please note if this role isn’t for you but you know someone who might like this role, we offer an iPad or new laptop for any referrals that lead to a placement

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If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.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.
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About Advanced

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.

Keywords / Key words: Regulatory, Regulatory Affairs, Reg Affairs, RA, Regulatory jobs, RA jobs, Regulatory Affairs Jobs, Regulatory, Regulatory Affairs, Reg Affairs, RA, Regulatory jobs, RA jobs, Regulatory Affairs Jobs.

To Apply : Please send a full CV in confidence to cv@advregulatory.com.

Contact Information:

Address:  Head Office
Suite 8 Penhurst House 352-356 Battersea Park Road London
SW11 3BY
England
Tel:  +44 (0)20 7801 3380
Fax:  +44 (0)20 7228 1188
Website:  Visit Our Web Site

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