| 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 | City of London |
| Education | Not Mentioned |
| Salary | 80.00 - 100.00 per hour |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Contract , full-time |
* Pharmacovigilance, Associate Director - Global Pharma - 12-month contract -OUTSIDE IR35* My client is a Global Pharmaceutical company and they have a position available for an Associate Director, Pharmacovigilance Safety Science to join their team for an initial 12-month contract.OUTSIDE IR35Within this role you will be accountable for all aspects of safety science/pharmacovigilance, you will support early and late phase development activities, providing essential safety oversight and input into all aspects of study management across the entiredevelopment and marketed portfolio. In the post-market setting this may include signal evaluation, safety related activities associated with new drug applications/regulatory filings, benefit-risk assessment and safety risk management.The Associate Director will be expected to work with minimal supervision and apply strong self-leadership.In order to apply for the Associate Director, Pharmacovigilance Safety Science contract, you should possess experience of working in the Pharmaceutical Industry in the field of pharmacovigilance with a strong knowledge of GxP and regulated processes and endto end clinical trial lifecycle. You will possess hands on experience of writing aggregate reports and have a good knowledge of Signal management activities. You will possess excellent written and verbal communication skills and be able to communicate withhealth authorities and stakeholders. Before you apply for this position it is vital that you are in possession of an UK passport or relevant visa to work without restrictions in the UK. You must be based 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
Keyskills :
PharmaceuticalPharmacovigilanceRisk ManagementRMPStrategyGxPPSURAssociate DirectorContractPhDPhysicianDSURaggregate reportssignal evaluationSignal Management