Reference Number: JO-2104-467515
Senior Associate Regulatory Operations
Rate: Negotiable
Job Type: Contract
Location: Central London / West End

Senior Regulatory Affairs Associate

6 month contract

Remote based

Offering up to 32.00 Per Hour DOE via Umbrella

Our client an internationally recognized pharmaceutical firms seeks a Senior Associate of Regulatory Operations on a 6 month contract basis. Supporting the Regulatory Operations team you will be responsible for facilitating product development and global registration through the efficient preparation, management and tracking of regulatory documentation and submissions.

Job Responsibilities include;

– Work as part of a global Regulatory Operations team, contributing to global filings
– Lead key submissions for EU, Switzerland and Emerging Markets
– Compilation and publishing of submission dossiers for Europe and the extended EU markets for clinical trials, paediatrics and marketing applications according to regional regulatory agency guidance
– Work closely with submission content providers to advise on submission content, structure, planning and strategy
– Submission management of publishing tasks sent to publishing vendors

Candidate Requirements include;
– Individual must be eligible to live and work in the United Kingdom
– Life Sciences degree or equivalent
– Prior experience with Regulatory Operations including regulatory publishing
– Good written and verbal communications
– Minimum 1-2 years working in a Regulatory Operations environment

If this position is of interest please forward your CV to sophie.malyon@cpl.com.