Regulatory Publishing & Submissions Jobs in UK

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Regulatory Affairs Manager

Salary:
£50k - £55k pa
Location:
Scotland
Job Type:
Permanent
Date Posted:
24-May-2012 10:44Add to My Shortlist

Role: -Management of compliance with relevant regulatory legislation and guidelines. -Defining project and product regulatory strategy of the Development Group in line with commercial and company strategy, consulting with appropriate departments where necessary. -Management of the production of paper and electronic regulatory submissions including applications for clinical trials and marketing authorisations. -Management of the provision of information requested by regulatory...

Oncology Regulatory Affairs Manager

Salary:
Neg
Location:
Uxbridge
Job Type:
Contract/Interim
Date Posted:
24-May-2012 17:00Add to My Shortlist

My client seeks to deliver truly innovative and life-changing drugs for their patients. Their mission is to build a major global biopharmaceutical corporation while focusing on the discovery and the development of products for the treatment of cancer and other severe, immune, inflammatory conditions. They are currently recruiting for an Oncology Regulatory Manager to work a 12 month Fixed Term...

Senior Regulatory Affairs Consultant - CMC

Salary:
£25 - £60 p hour
Location:
Hertfordshire
Job Type:
Contract/Interim
Date Posted:
24-May-2012 00:00Add to My Shortlist

A Global Pharma company are presently looking to bring in a Senior Regulatory Affairs Consultant to their CMC group, 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...

Regulatory Affairs Consultant - CMC

Salary:
£25 - £60 p hour
Location:
West London
Job Type:
Contract/Interim
Date Posted:
24-May-2012 00:00Add to My Shortlist

A Global Pharma company are presently looking to bring in a Regulatory Affairs Consultant and also a Senior Regulatory Affairs Consultant for their CMC group, 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....

Regulatory Affairs Director

Salary:
Competitive Salary
Location:
Surrey
Job Type:
Permanent
Date Posted:
19-May-2012 00:00Add to My Shortlist

Primary Goal Responsible for directing all regulatory activities and developing and implementing strategies for timely approvals of Phase I through Phase IV clinical trial applications; counselling and overseeing regulatory teams; ensuring timely preparation and submission of regulatory documentation to European and international drug regulatory authorities; ensuring the quality, content and format of regulatory submissions; and interacting with regulatory agencies, project...

Medical Device Senior Regulatory Affairs Officer

Salary:
Neg
Location:
Edinburgh
Job Type:
Permanent
Date Posted:
25-May-2012 08:47Add to My Shortlist

My client is a major bio-manufacturing organisation, supplying vital products to hospitals, blood services and healthcare companies in over 30 countries. They are currently recruiting for Senior Regulatory Affairs Officer to work across their in-vitro diagnostic product range at their offices in Edinburgh. Main duties of the role will be to manage, prepare and maintain regulatory documentation to enable the...

Regulatory Associate

Salary:
£20.00 - £40.00 p hour
Location:
Surrey
Job Type:
Contract/Interim
Date Posted:
21-May-2012 17:44Add to My Shortlist

Regulatory Associate Weybridge 6 Month Contract from £20 per hour Preparation of high quality, detailed regulatory documents using varied information sources. Liaising closely with other internal personnel to ensure accuracy of such records. Working to agreed deadlines and maintaining records reflecting project status. Responsible for highlighting potential delaying factors promptly to line management and sharing knowledge of regulatory documentation and procedures...

Senior Regulatory Affairs Consultant

Salary:
£35,000 + Bonus package
Location:
Livingston, Edinburgh
Job Type:
Permanent
Date Posted:
23-May-2012 00:00Add to My Shortlist

Senior Regulatory Affairs Consultant - £35,000 + bonuses Our client develops and manufactures specialist products for the global bio-market. Due to steady expansion they have an opportunity for a Senior Regulatory Affairs Consultant to join their team and be a part of their continuing growth. The Senior Regulatory Affairs Consultant will be responsible for: The preparation and maintenance of the...

Regulatory Submissions Manager

Salary:
£45k - £55k + benefits
Location:
London, Kent, Uk
Job Type:
Permanent
Date Posted:
23-May-2012 12:23Add to My Shortlist

Our client, an innovative and rapidly expanding Clinical Research Organisation are looking for experienced Regulatory Submissions Managers to come and join their busy team in South-East London. Your role will be to efficiently manage and successfully execute all aspects of global start-up according to Sponsor specifications, perform quality checks on submission documents and site essential documents, interact with central IRBs, ...

Associate, Documentation Quality Regulatory Affairs

Salary:
£Negotiable + Benefits
Location:
Hertfordshire, London, Middlesex, Cambridgeshire, Bedfordshire
Job Type:
Any
Date Posted:
19-May-2012 00:00Add to My Shortlist

Associate, Documentation Quality Regulatory Affairs Location: Hertfordshire Employment term: Permanent Salary: Competitive A fantastic opportunity has arisen for a Associate for Documentation Quality, Regulatory Affairs to join a global pharmaceutical company based in Berkshire. The Associate for Documentation Quality, Regulatory Affairs will support the Medical Writers and Regulatory Affairs Authors to ensure data accuracy and formal quality in the documentation...

Regulatory Affairs Associate

Salary:
On Application
Location:
London, Bedfordshire, Hertfordshire, Buckinghamshire, Cambridgeshire, England
Job Type:
Permanent
Date Posted:
25-May-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 Regulatory Affairs Associate with a proven track record working in regulatory affairs and quality assurance in the UK or EU. The main responsibilities in this...

Regulatory Documentation Scientist

Salary:
On Application
Location:
Essex, Hertfordshire, London, Middlesex
Job Type:
Permanent
Date Posted:
24-May-2012 09:14Add to My Shortlist

JOB SUMMARY: Here is a great opportunity to combine your scientific knowledge and writing skills in an important role with one of the world's leading healthcare companies. You will be responsible for the project management and preparation of vital safety regulatory reports for innovative products and part of a global team driving the development of our clients rich pipeline of...

Medical Devices Regulatory Submissions Manager - Belgium

Salary:
€47,500 - €57,500
Location:
Mechelen, Brussels, Leuven, Belgium, Uk, England, Scotland, Stirling
Job Type:
Permanent
Date Posted:
24-May-2012 18:59Add to My Shortlist

Craig Edwards from Meet is pleased to present this fantastic new opportunity to you - for those who currently work as, or aspire to be: *Regulatory Submissions Manager (2-Senior) Medical Device experience needed ***************************************************** A Rapidly expanding, ambitious Global CRO with global locations. Regulatory Submissions Manager vacancies in the UK and Belgium. You will be required to effectively manage projects, ...

Regulatory Affairs Manager

Salary:
£45k - £55k pa
Location:
Cambridgeshire
Job Type:
Permanent
Date Posted:
21-May-2012 14:26Add to My Shortlist

Overall function of the job To implement the Company's regulatory strategy To ensure the Company has compliance to the regulations of the national, European and global regulatory authorities, including USA (FDA) Preparing submissions of approvals, variations and renewals Ensuring documentation is generated and stored in compliance with the requirements for regulatory submission To take responsibility for planning and implementing clinical...

Regulatory Affairs Associate - Ukraine

Salary:
negotiable
Location:
Maidenhead, Berkshire
Job Type:
Permanent
Date Posted:
19-May-2012 00:00Add to My Shortlist

In the complex world of drug development, PharmaNet/i3 is exactly where you need to be. With offices in more than 30 countries around the world, PharmaNet/i3 has the resources to conduct any study; from a large multi-country, multi-language clinical trial today, to a smaller regional study tomorrow. PharmaNet/i3 works for you on trials of any size, anywhere around the world....

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