Regulatory Publishing & Submissions Jobs in Europe
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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...
Clinical Trials / Submissions / Regulatory Specialist - Netherlands
- Salary:
- €27000 - 45000
- Location:
- Netherlands, Amsterdam
- Job Type:
- Permanent
- Date Posted:
- 23-May-2012 17:51Add to My Shortlist
*Clinical Trial Specialist *Submissions Specialist *Start-up Associate *Regulatroy Coordinator ______________________________________ This leading global CRO with offices in Netherlands can offer you home/office flex, reward experience with top salarys and help you meet your development goals ROLE RESPONSIBILITIES: Update tracking systems, follow up on site related queries and submit documentation to satisfy safety updates, as well as completing routine administrative tasks...
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...
Regulatory Submissions Leader circa €55, 000 Netherlands
- Salary:
- €45000 - 55000
- Location:
- Netherlands, Amsterdam
- Job Type:
- Permanent
- Date Posted:
- 18-May-2012 17:06Add to My Shortlist
*Lead SSU *Study start-up Lead *Clinical Submissions leader Full company details and job description are available upon application; no CV is submitted until full discussion has taken place. Please contact Craig Edwards at Meet on +44 203 178 7488 or email craig@peoplewithchemistry.com Contact via LinkedIn: [URL removed] Meet are good people who are great at recruitment. We're proud to partner...
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:
- €36k - €38k + benefits
- Location:
- Leuven, Belgium
- Job Type:
- Permanent
- Date Posted:
- 23-May-2012 13:20Add 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 Leuven. 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, sites, ...
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...
