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Regulatory Affairs Associate - 12 month contract

Business Type: Clinical Research Organisation
Job Type: Clinical - Drug Safety, Quality Assurance - Control, Clinical Study- Trials, Regulatory Affairs
Job Level: Not Specified
Position: Contract
Salary: Competitive
Location: East Anglia
Reference: 17860/001
Closing Date: 14/08/12

Our client is a world leading company aspiring to be the best in the discovery and development of important therapeutics. They are currently seeking a Regulatory Affairs Associate for a 12 month contract at their Cambridge site.

The Regulatory Affairs Associate will support regulatory filing by authoring Regional Prescribing Information (RPI) source text for Europe (EU) , Switzerland and Emerging Markets (EM) and will ensure timely availability of correct RPI source documents.

Proven proof reading skills
Familiar with document management systems and process
Previous labelling experience would be essential
Broad knowledge of regions including EU and US

Proficiency in Microsoft Word
Excellent communication skills

BENEFITS OF THE ROLE: Our client offers an outstanding work environment with a culture based on a deep respect for individual talent and a value system which ensures that every person has the opportunity to make a significant difference.

Fforde is acting as a recruitment agency/business.

KEY WORDS: Regulatory Affairs Associate, Drug Development, Drug Safety, Clinical Trials, Proof reading, Clinical Research, Emerging Markets, Regulatory, Labelling, Contract, Cambridge

Posted: 17/07/2012 | NPJ Ref: 84188
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