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| Job Location | Windsor |
| Education | Not Mentioned |
| Salary | £55.00 - £70.00 per hour |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Contract, full-time |
*Senior Pharmacovigilance Safety Scientist - Global BioPharma - 6-month contract* My client is a Global Biopharmaceutical company and they have a position available for a Senior Pharmacovigilance Safety Scientist for an initial 6- month contract.Within this role the Senior PV Scientist serves as a product lead for Pharmacovigilance activities they are responsible for overseeing and leading the process for safety signal management activities, aggregate reports responding to safety questions from internal and external stakeholders, reviewing medical and scientific literature for safety information, and supporting Clinical Trial PV medical activities. The Senior PV Scientist also serves as a Subject Matter Expert on relevant global safety regulations and guidelines; data output and analyses; and product specific information.In order to apply for the Senior Pharmacovigilance Safety Scientist contract, you should possess extensive experience in the field of pharmacovigilance within the Pharmaceutical industry, including experience in writing aggregate safety reports and safety signal management. You should possess a strong background in clinical trial drug safety and be able to understand, interpret, analyse, and clearly present scientific and medical data in verbal and written format (including intermediate understanding and application of medical concepts and terminology).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 :
Pharmacovigilance RMP PV PSUR contract Risk management Signal detection aggregate repts signal management Aggregate rept writing PBERs