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Fforde Management
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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: UK - East Anglia
Reference: 17860/001
Closing Date: 14/08/12
Background:

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.

JOB ROLE:
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.

QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
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

PERSONAL SKILLS & ATTRIBUTES:
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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