Regulatory Publishing & Submissions Jobs in Regulatory Affairs

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Regulatory Affairs Submissions Publisher

Salary:
£20 - £40 p hour
Location:
London
Job Type:
Contract/Interim
Date Posted:
07-Feb-2012 00:00Add to My Shortlist

A Global Pharmaceutical company are presently looking to bring in a Regulatory Affairs Submissions Publisher to be based in the UK London Office, on a contract basis. Role: - Contributes toward the delivery of paper and electronic submissions - Creation and co-ordination of publishing strategies - Hypertext linking and QC checking - Documentum based document management systems - Aligns Regulatory...

CMC Senior Regulatory Executive

Salary:
£50 - £70 p hour
Location:
South East England
Job Type:
Contract/Interim
Date Posted:
11-Feb-2012 00:00Add to My Shortlist

Job Title : CMC Senior Regulatory Executive Location : Middlesex , South East England Contract Rate : £50-£70 per hour depending on experience Contract Length : 12 Months + possible extensions A Senior Regulatory CMC specialist with strong documentation experience is required by a leading Pharmaceutical company based in the Greater London area. The ideal candidate will be responsible for...

Regulatory Affairs Associate

Salary:
£25 - £35 pa
Location:
Weybridge
Job Type:
Permanent
Date Posted:
11-Feb-2012 00:00Add to My Shortlist

Job title: Regulatory Affairs Associate Job type: 6-12 month contract + extensions Location: Weybridge, Surrey Salary: £25 to £35/hour A Regulatory Affairs Associate with Medicinal Product experience is required by a leading Pharmaceutical / Healthcare company based in the Weybridge area The ideal candidate will be responsible for taking ownership of regulatory licenses, as well as compiling detailed documentation In...

Regulatory Affairs Consultant

Salary:
£35 - £60 p hour
Location:
West London
Job Type:
Contract/Interim
Date Posted:
07-Feb-2012 00:00Add to My Shortlist

A Global Pharma company are presently looking to bring in a Senior Regulatory Affairs Executive within the EU team to be based in the UK West London Office, on a contract basis. Role: - Preparation of high quality, chemistry manufacturing and control (CMC) detailed regulatory documents using varied information sources. - Liaising closely with other personnel to ensure accuracy of...

Regulatory Affairs Associate - CMC Submissions

Salary:
On Application
Location:
Hertfordshire, East
Job Type:
Any
Date Posted:
11-Feb-2012 00:00Add to My Shortlist

i3 are currently recruiting for a Regulatory Affairs Associate for a regulatory affairs opportunity dealing with CMC Submissions. This is a great opportunity for someone to develop their experience within CMC Regulatory Affairs and work in an established Regulatory Affairs department of a world leading company, based in Hertfordshire. Working as a Regulatory Affairs Associate you will provide Quality Assurance...

Regulatory Affairs Associate - Consumer Health

Salary:
On Application
Location:
Surrey, South East England
Job Type:
Any
Date Posted:
11-Feb-2012 00:00Add to My Shortlist

i3 are currently recruiting for a Regulatory Affairs Associate for a regulatory affairs opportunity dealing with Consumer Health products. This is a great opportunity for someone to develop their experience across a broad range of products and work in an established Regulatory Affairs department of a world leading company based in Surrey. As Regulatory Affairs Associate you will primarily be...

Regulatory Affairs Manager

Salary:
Neg
Location:
South East England
Job Type:
Contract/Interim
Date Posted:
10-Feb-2012 13:52Add to My Shortlist

Job Summary: Within this role you will work to define the commercial objectives and provide regulatory guidance and precedence for the International region. You will also guide the development of the International components and provide guidance on regional regulatory mechanisms to optimize product development. Key Activities: -Support core regulatory activities to ensure effective regional agency interactions consistent with the Global...

Regulatory Affairs Manager and Specialist

Salary:
TBC + Benefits
Location:
Brussels
Job Type:
Permanent
Date Posted:
09-Feb-2012 00:00Add to My Shortlist

PPD is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. We are seeking a Regulatory Affairs Manager to be based from our offices in Brussels. The Regulatory Affairs Manager is required to provide regulatory advice on strategy and manage projects in...

Regulatory Affairs Director

Salary:
On Application
Location:
London, Bedfordshire, Hertfordshire, Buckinghamshire, Cambridgeshire
Job Type:
Permanent
Date Posted:
10-Feb-2012 00:00Add to My Shortlist

Novella Clinical is a global, full service CRO with European Headquarters in Hertfordshire, England. We are committed to providing a superior service to our global clients, and as such we are seeking hire an experienced a Senior Regulatory Affairs professional with a proven track record working in regulatory affairs on a and quality assurance, at a Global Level The Regulatory...

Regulatory Submissions Manager - Poland

Salary:
On Application
Location:
Poland, Warsaw, Krakow
Job Type:
Permanent
Date Posted:
08-Feb-2012 00:00Add to My Shortlist

Regulatory Submissions Manager - Poland Job Summary: Regulatory Submissions Manager - Poland This role requires the candidate to efficiently manage and successfully execute all aspects of global submissions according to Sponsor specifications. The role is based around the achieving of successful submissions from sites in accordance with regulations, requirements, and SOPs. Requirements: Regulatory Submissions Manager - Poland * Assist Clinical...

Senior Regulatory Associate

Salary:
Neg
Location:
South East England
Job Type:
Contract/Interim
Date Posted:
10-Feb-2012 09:41Add to My Shortlist

Overview: Within this role you will be responsible for preparing and filing necessary regulatory documents for clinical trial applications and handling interactions with clinical study teams and regulatory LOCs/Hubs regarding clinical trials activities. The activity also includes maintenance activities such as dealing with amendments/notifications and questions from CAs. - Ensure creation and maintenance of adequate regulatory clinical trial activities trackers....

Regulatory Affairs Specialist (Medical Device / Medical Systems)

Salary:
£40K - £45K + Benefits
Location:
West Sussex, East Sussex, Kent, Surrey, London, Hampshire, Redhill, Reigate, Tonbridge, Croydon, Brighton, Maidstone, Bromley, Guildford, Horsham, Worthing, Crawley
Job Type:
Permanent
Date Posted:
09-Feb-2012 00:28Add to My Shortlist

Regulatory Affairs Specialist -Medical Device / Medical Systems- £40K - £45K + Benefits **An excellent opportunity for a Regulatory Affairs Specialist with a background in medical devices, healthcare or pharmaceutical production to join a market leading supplier of sophisticate medical systems** The Company, Regulatory Affairs Specialist, Medical Device / Medical Systems My client is a worldwide market leading supplier of...

Regulatory Submissions Manager - EU

Salary:
On Application
Location:
Poland, Europe, Krakow, Warsaw, Berlin, Germany, Slovakia, Slovenia, Estonia, Lithuania, Czech Republic, Bulgaria
Job Type:
Permanent
Date Posted:
10-Feb-2012 16:49Add to My Shortlist

Regulatory Submissions Manager - Poland Job Summary: Regulatory Submissions Manager - Poland. This role requires the candidate to efficiently manage and successfully execute all aspects of global submissions according to Sponsor specifications. The role is based around the achieving of successful submissions from sites in accordance with regulations, requirements, and SOPs. Requirements: Regulatory Submissions Manager - Poland * Assist Clinical...

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