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Job Details

Regulatory Affairs, Global Regulatory Lead, Associate Director, Early Development

Company: Advanced Regulatory (UK & Europe)
Location: UK, M4 Corridor
Reference: MGADV / 10346
Closing Date: 09 Mar 18
Type: Full Time
Salary (£): On Application
Benefits: On Application

Job Summary:

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.

Requirements:

Regulatory Affairs, Global Regulatory Lead, Associate Director, Early Development

Location: : South-East, M4 Corridor, West London

Home working options available.

Our successful global Pharmaceutical client is fairly unique, they offer individuals a career ladder with global regulatory leading (GRL) positions, based right here in Europe, within their EU HQ in the UK (South-East/M4 Corridor) but with options to work 2 days a week from home.

This organisation has a bright outlook, due to many recent successes achieved from a well-funded, rich and diverse pipeline and a senior management team which is committed to providing patients, customers, community and employees a bright future with their patient centric approach to product development .


They are now offering new opportunities to join their Global Early Development Team, in a role where you can utilise your strong leadership experience and where regulatory is seen as a valued, strategic partner.

As the Global Regulatory Affairs Leader (GRL) you will provide regulatory leadership to assigned asset(s) & leading the global Regulatory Strategic Team for assigned projects. This role will be accountable for the global regulatory strategy and oversight of implementation/execution in alignment with the Regional Regulatory Leads for Early Medicines.

If you are looking for an organization that is moving in the right direction in a role that is visible and highly strategic, then this could be the company for you…!!!

Ideally you will strong experience around development, CTA’s, PiPs, ODD’s, Scientific advice and MAA’s via Centralised and/or De-Centralised procedure.  The packages are exceptional and include a comprehensive re-location for those who may need it, an exceptional salary, Car/Car allowance, Bonus up to 20%, share options worth and additional 20k a year.

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To be considered for the above roles (available to any individual eligible to work in the EU including those individuals requiring relocation) please call Theo Moore or Matt Greig, on +44(0)207 801 3384 or +44(0)7918 195 166, alternatively send a full CV to cv@advregulatory.com
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Advanced Referral Scheme - We also offer an iPad 3 for any referrals that we help to place into a new role, so if this role isn’t for you, then please think about referring a friend or colleague…Many thanks…!!!

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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, GRL, Global Regulatory Lead, Regulatory Affairs Jobs UK, UK Pharmaceutical 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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