Job Overview

Apply now *Senior Pharmacovigilance (PV) Business Analyst, Top 10 Pharmaceutical, 16 month contract, Buckinghamshire* My client a leading Pharmaceutical company is currently looking for a Pharmacovigilance Business Analyst to join their team.Your new role As the Senior PV Business Analyst you will be responsible for the management of the User Requirements process for Global Medical Safety (GMS) PV system enhancements, ensuring user requirements are clearly defined, documented, approved and tested. You will be responsible for leading the user acceptance testing phase for PV systems enhancements, ensuring business partner participation throughout the process, including test script review and approval, test script execution and go-live approval. Providing support to GMS and external partners on PV systems, processes and interfaces, implementation of new systems, systems upgrades and management of the change process. You will have ownership and development of new and existing PV systems Training Material in line with new systems and releases. As the Senior PV Business Analyst, you will investigate and implement innovative solutions that provide enhanced compliance, efficiency and quality to PV processes, PV systems and interfaces. What you'll need to succeed Test scriptingImplementing new systemsSupporting GMS (Global Medical Safety) and external stakeholdersPharmacovigilance - processes & systemsManaging and developing new and existing training materialUAT (User Acceptance Testing) ManagementCAPA ManagementPV Audits and Inspections What you need to do nowBefore you apply for this position it is vital that you are in possession of an EU or UK passport or relevant visa to work without restrictions in the UK. If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Roberta on .If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.

Key Requirements

Compliance Drug Safety EMA FDA Pharmacovigilance QA Quality Assurance Risk Management MHRA PV CRO Pharmaceuticals Medical Information Generics Clinical Safety ARGUS AE Case Processing Case Reporting Adverse Event ARISG