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 Publisher for a 5 month contract at their Cambridge office.
JOB ROLE:
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;
Teamwork;
Problem solving;
Strong written and verbal communication skills;
Computer Competency
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