Reference Number: JO-2011-458248
Regulatory Consultant
Rate: Negotiable
Job Type: Contract
Location: Central London / West End

Regulatory Affairs Consultant
Interim contract between December 2020 – March 2021
Fully Home based
Attractive Hourly Rate

CPL Life Sciences is currently collaborating with a leading gene therapy biotechnology organisation who seek an experienced Regulatory Affairs Consultant on a interim between December 2020 to March next year. The ideal candidate will have availability to start early December.

Reporting into the Senior Director of Regulatory Affairs this position will be very operational focused, with tasks involving mostly centralised procedure and post approval procedures (variations, PASS and CMA renewals). This individual will also be responsible for country support throughout Europe including affiliate regulatory set-up and Educational Material preparation and submission.

Candidate Requirements include;
– Individual must be eligible to live and work in either the United Kingdom or Switzerland
– A minimum of 5 years Regulatory Affairs experience
– Prior experience working within centralised procedure
– Prior experience with biologics would be highly advantageous

If this position is of interest to yourself please call Sophie at CPL Life Sciences on 07526 003 117 or alternatively forward your CV to sophie.malyon@cpl.com.

Upload your CV and any other relevant file.
I would like to be contacted via SMS
I have read and agree to the Clinical Professionals Group Privacy Policy

Find our privacy policy here