Regulatory Publishing & Submissions Jobs in M4 Corridor

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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 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....


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...


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