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| Job Location | London |
| Education | Not Mentioned |
| Salary | Competitive salary |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
Pharmacovigilance Scientist role with a London based market leading CRO I am working with a market leading CRO located in London that specialise in early phase trial management, who are now searching for a Pharmacovigilance Specialist to join their close-knit team. This is an opportunity that will provide you with a lot of exposure, valuable knowledge, growth, and progression with the company. You will be surrounded by very experienced and likeminded individuals and liaise closely with the companys research physicians, clinical teams, and other stakeholders. Your main responsibilities will include (but are not limited to): - Manage the reporting of SAEs for clinical trials - Quality control services within the safety reporting team - Liaise closely with other stakeholders of the company - Contributing to signal detection activities - Assist management in the implementation and improvement of operational processes - Ensuring compliance (quality, procedures, regulations, timeliness, consistency) with local regulations and companys pharmacovigilance requirements - Audit and inspection readinessTo succeed in this role, you should have previous dealings with the above, a strong background in drug safety from a CRO, pharmaceutical or consultancy background and strong knowledge of GVP and GDP. To apply for this exciting PV Scientist role and have the opportunity to work with great people in a transparent environment, click apply now to forward an up to date copy of your CV, or call us now. If this job isnt quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Required skills
Keyskills :
CRO seni Life Science pharmaceutical clinical officer specialist clinical trials scientist pharma drug safety pharmacovigilance pv physician biotech associate case processing