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 Publisher for a 5 month contract at their Cambridge office.
The Regulatory Publisher will facilitate product development and global registration through the efficient preparation, management and tracking of regulatory documentation and systems
PRINCIPAL RESPONSIBILITIES include:
Formatting and publishing of regulatory documentation for submission
QC of regulatory dossiers
Preparation and despatch of media for regulatory submissions and/or
Management of regulatory documentation and information
QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
Previous regulatory publishing experience within the pharmaceutical industry
Use of specialist publishing software to prepare submissions and electronic document management systems
PERSONAL SKILLS & ATTRIBUTES:
Attention to detail;
Strong written and verbal 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, Publisher, Clinical Research, Clinical Trials, Regulatory Affairs, Pharmaceutical, Publishing, Degree, Contract, Cambridgeshire