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USA NEW REGULATORY ROLE *** Regulatory Manager *** Learn RA strategy & lead your NMEs in your region *** RTP or ATL, USA

Company: Advanced S&S (USA)
Location: US Home OR RTP, or ATL
Reference: MGADV / 280817H
Closing Date: 23 Nov 17
Type: Full Time
Salary (£): On Application
Benefits: On Application

Job Summary:

Generous relocation is offered! And both RTP and ATL, offer lower cost, higher quality housing than Mid West and Tri State areas, but most of all, these roles are within a company which is expanding, and can offer you many steps in your career!

Requirements:

USA NEW REGULATORY ROLE *** Regulatory Manager *** Work on bio/NCEs in early phase global dev ** learn RA strategy & lead your NMEs in your region *** RTP or ATL, USA

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You will be an experienced Senior Associate, Specialist, or Manager, and be willing to either work in Research Triangle Park, North Carolina, or in Atlanta, Georgia. Individuals with several years’ experience and wanting this type of role from home, for a home working permanent contract, can also apply.

Generous relocation is offered! And both RTP and ATL, offer lower cost, higher quality housing than Mid West and Tri State areas, but most of all, these roles are within a company which is expanding, and can offer you many steps in your career!

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My client has a strong portfolio and is an expanding medium sized bio-pharma with new products on the market, and now wanting to take their pipeline up a gear of 2. The global regulatory team is led by ex-Roche, Wyeth and AZ people, and has a culture of merit-based advanced.

The teams are working on a global matrix led by Global Regulatory Leads, and this is one of the ultimate development pathways you will be encouraged to develop into. The company has many examples of people who have developed up including the line manager who you will be reporting to.

This role is to work with R&D to bring your assigned NMEs, a mix of small and large molecules, into Phase 1 and through to 2a and 2b, at which time you may follow one of your NMEs through, if it receives Ph 3 Go decision.

You will develop US INDs, global CTAs, filed mostly through CROs, and CRO / vendor management experience us useful (as is CRO Regulatory experience as one option), co-develop regulatory strategy documents including interfacing with the global clinical development and commercialization teams, as well as prepare Pre-IND, EOP2, and other HA meetings.

My client is seeking someone who is ‘hands-on’ and has authoring / writing skills for INDs, and other regulatory documents, although you will be supported by Clin / non-Clin, this role requires this. Outside this idea, GRA CMC authors CMC documentation for you.

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Advanced Regulatory part of Advanced Search, are supporting this hiring process and will help you every step of the way. We do not require any bank or personal information, and our services are paid for by the customer (the hiring organization).

We invite you to apply for this role, by contacting myself or my colleague, Matt Greig or Theo Moore, at Advanced Regulatory (part of Advanced Search and Selection). We will support you with a fast, fair and positive hiring process.

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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 or dial Toll Free from the US on 855 505 1382.
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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)207 801 3380
Website:  Visit Our Web Site

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