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.
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