London Jobs |
Manchester Jobs |
Liverpool Jobs |
Nottingham Jobs |
Birmingham Jobs |
Cambridge Jobs |
Glasgow Jobs |
Bristol Jobs |
Wales Jobs |
London Jobs |
Manchester Jobs |
Liverpool Jobs |
Nottingham Jobs |
Birmingham Jobs |
Cambridge Jobs |
Glasgow Jobs |
Bristol Jobs |
Wales Jobs |
Oil & Gas Jobs |
Banking Jobs |
Construction Jobs |
Top Management Jobs |
IT - Software Jobs |
Medical Healthcare Jobs |
Purchase / Logistics Jobs |
Sales |
Ajax Jobs |
Designing Jobs |
ASP .NET Jobs |
Java Jobs |
MySQL Jobs |
Sap hr Jobs |
Software Testing Jobs |
Html Jobs |
Job Location | Maidenhead |
Education | Not Mentioned |
Salary | £25.00 - £26.00 per hour |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Contract, full-time |
Duration: 12 month ContractLocation: Maidenhead, Berkshire (Remote initially, with 1-2 days in the office when able)Salary: c.26.00 per hour (c.195 per day) - PAYE onlyHours: 7.5 per day (37.5 hours weekly)Starting Date: Jan/Feb 2021Our 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