Regulatory Publishing & Submissions Jobs in South East
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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...
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...
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 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 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...
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 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....
Senior Manager Regulatory Affairs
- Salary:
- On Application
- Location:
- Berkshire, Oxfordshire, London, Surrey, Wiltshire, Hampshire, Middlesex
- Job Type:
- Permanent
- Date Posted:
- 19-May-2012 00:00Add to My Shortlist
JOB SUMMARY: Fantastic opportunity for an experienced Regulatory Affairs specialist to take responsibility for management of Regulatory Affairs activities relating to one or more products. You will also be responsible for obtaining and maintaining the required regulatory approvals for those products, including clinical trial approvals and provide strategic regulatory advice to project teams in relation to product development (manufacturing, safety, ...
Regulatory Affairs Manager - Oncology
- Salary:
- negotiable
- Location:
- Stockley Park, Uxbridge, Uk
- Job Type:
- Contract/Interim
- Date Posted:
- 24-May-2012 12:18Add to My Shortlist
Responsibilities will include, but are not limited to, the following: * Work with the Global Regulatory Functional team and EU Regulatory strategy leaders to implement regulatory plans for development and post licensing projects in the EU region. * Provide input on the European regulatory plans to project teams during all phases of the product life-cycle. * Give regulatory input to...
