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Job Details

R E G U L A T O R Y *** Do you have US exposure or exp >> Now want to be a GRL? ** W London / M4 Corridor ** Grade Assoc Director or Director **

Company: Advanced Regulatory (UK & Europe)
Location: M4/M40/M25 W London
Reference: MGADV / 30318 /A
Closing Date: 12 Apr 18
Type: Full Time
Salary (£): 100,000+
Benefits: Package Quoted

Job Summary:

R E G U L A T O R Y *** Do you have US exposure or experience and now want to be a GRL? ** West London / M4 Corridor ** Grade Associate Director or Director ** Package includes Stock, Bonus, Car Allowance


R E G U L A T O R Y *** Do you have US exposure or experience and now want to be a GRL? ** West London / M4 Corridor ** Grade Associate Director or Director ** Package includes Stock, Bonus, Car Allowance


I am now hiring for an experienced regulatory strategist and regulatory project manager. You will have already established your career level as a Regulatory Liaison or RA Leader, and now want to establish yourself on the global strategy level where you are responsible for the global strategy document, and for co-defining with the partners, the clinical development and regulatory pathway for NMEs in early phases (this group is not therapeutically aligned and cover a broad spread of diseases).

This role is not for someone who wants to do line extension filing after line extension filing (call me if you want this as I have other roles), because this is role which is more focused on developing the value for the molecule in early development, identifying potentials for speedier or parallel development, adaptive or innovative pathways, hence is more conceptual in this respect.

Personality wise, you will have a friendly and engaging personality, willing to work with the scientists, medics, tox and stats experts to generate new ideas and shape existing ones. You will be a team player, but know how to influence individuals to steer programmes, in a company which has a strong matrix.

Experience-wise, US exposure is useful, as you can imagine, but the requirement is you have some actual early phase development experience, in regulatory, and understand how regulatory can lever their know-how to drive drug development, initiate and manage useful health authority interactions, and prime the molecule for commercialization in Phase 3. You will have a big voice on the POC decisions at end of Ph 2 and will lead in this role all US, EU and China / Japan regulatory plans and agency interactions (in a global matrix, with affiliate partners in some cases).

We have options on grade, so you can be interested in either an Associate Director or Director grade, and be based in the West of London, Bucks, Berks, Middlesex areas. Some home working is available for this role.


To apply for this role, please send your CV with a covering note to 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)2078013380 or +447918679405 (eves / weekends).


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

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.

To Apply : Please send a full CV in confidence to

Contact Information:

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

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