Overview

Reference Number: JO-2011-459010
Regulatory Affairs Systems Specialist
Rate: Negotiable
Job Type: Contract
Location: Maidenhead

Duration: 12 month Contract
Location: Maidenhead, Berkshire (Remote initially, with 1-2 days in the office when able)
Salary: c.26.00 per hour (c.195 per day) – PAYE only
Hours: 7.5 per day (37.5 hours weekly)
Starting Date: Jan/Feb 2021

Our Client, a large global pharmaceutical business is seeking a Regulatory Affairs System Specialist for an initial 12 month contract to provide essential project management support to the Global Regulatory Affairs’ in-flight electronic document management system upgrade project. In particular, the Candidate will support the system Business Process Owner with business analysis activities, requirements definition, system validation documentation, UAT script creation / execution and training development and delivery.

Skills:
We are looking for Candidates well versed in supporting large scale electronic document management system implementation / upgrade projects with 2-3 years experience of Documentum Life Sciences D2 and Veeva Submissions Vault within the pharmaceutical Regulatory business. You should have an understanding of project management approaches and should have a keen awareness of computerised system validation techniques and approaches.

If you feel you meet the criteria of the position, please submit your CV to Stephen Wincott at stephen.wincott@cpl.com

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