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 | Cambridge |
Education | Not Mentioned |
Salary | £33.00 - £41.00 per hour |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Contract , full-time |
Your new companyMy client, a Biopharmaceutical company that is focussed on development, commercialisation and discovery of innovative medicines, has an opportunity for a Senior Pharmacovigilance Scientist to join their Patient Safety team on an initial 6-month rolling contract. 3 days on-site at CambridgeInscope IR35Your new roleAs a Senior Pharmacovigilance scientist, you will perform operational job responsibilities that ensure compliance of pharmacovigilance activities including the collection, review, evaluation, processing, and submission of adverse event (AE) information receivedby the team.* Performs routine and non-routine daily case management activities independently and provides direction as needed to junior staff, assists junior staff as needed* Leads training and/or on-boarding activities* Leads projects of high complexity* Participates in cross-functional projects * May serve as a point of contact for other functions inside and outside the organisation* May develop and/or assist with quality review of data for the applicable functional areaWhat youll need to succeedYou will hold a Masters or Bachelors degree in life sciences and have substantial experience within Pharmacovigilance. You will be able to effectively represent PS Strategic Operations in multidisciplinary teams. You will have sound knowledge of pharmacovigilancelegislation and product development processes especially with ICSR processing, specifically with Argus, plus experience with vendor oversight.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 youre interested in this role, click apply now to forward an up-to-date copy of your CV, or call Roberta Atkins on If this job isnt quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.
Keyskills :
PharmacovigilanceContractvendor managementCambridgeArgusAdverse eventsICSR Case processing