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 | Great Abington |
Education | Not Mentioned |
Salary | Salary negotiable |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Contract, full-time |
*Pharmacovigilance Manager - Global Pharma - 12-month contract - Cambridge* My client is a Global Pharmaceutical company and they have a position available for an Pharmacovigilance Manager to join their team for a 12-month initial contract.Within this role you will be responsible for ensuring timely and appropriate safety exchange between the company and contracted CROs for their Sponsored Clinical Trials to meet Regulatory Reporting timelines in applicable countries. You will be responsible for following internal processes to ensure CTSRPs are sufficient to meet compliance with CT and GVP standards.In order to apply for the Pharmacovigilance Manager contract, you should possess a scientific degree and have experience of working in the Pharmaceutical Industry with previous experience in multiple aspects of pharmacovigilance activities. You will have excellent project management experience including managing complex projects and excellent knowledge of Global safety regulatory requirements. Proven good communication skills and the ability to work in cross functional teams is a must.Before 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.To apply for this position or if you want to discuss other roles that we are working on, please do not hesitate to contact Roberta Atkins on . Required skills
Keyskills :
Compliance Regulations PV contract legislation vend Cambridge ICSR patient safety Clinical trials PVE case processing Pharmacovigilace