The main purpose of the role as Pharmacovigilance Systems Manager will be to:
- Act as the subject matter expert for the PV systems in the EMEA region; including the maintenance of the validated PV systems
- Support local and regional users as systems administrator, providing technical expertise and training to Business Users for current and future PV system use
- Act as an interface between PV and IT and between PV and software vendors
Further responsibilities will include:
- Managing change control and validation to maintain Pharmacovigilance (PV) adverse event systems in compliance with the company’s guidance and SOPs
- Performing dry-run test scripts and User Acceptance Testing for any upgrades/changes
- Creating Business Intelligence reports for input into aggregate reports, audits/inspections
Your Background:
- To succeed in this role, you will come from an extensive background experience at administrator level with ARISg and electronic (E2B) reporting systems
- Relevant Pharmacovigilance experience linked to Computer system validation, as well as Reporting Applications such as Business Intelligence
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 56442 in all correspondence.