Accountabilities/Responsibilities:
-- Supporting pharmacovigilance activities
-- Setting up safety databases
-- Processing Serious Adverse Event reports
-- Acting as a mentor for pharmacovigilance team members
-- Participating in client liaison
-- Ensuring pharmacovigilance data is processed such that subjects rights, safety and well being are protected and that the pharmacovigilance data are reliable
Full job description available to see
Essential Skills & Capabilities:
Essential, 3 years pharmacovigilance experience including ASUR/PSUR and E2B reporting.
Preferred, CRO experience. Awareness of global regulatory environment and good awareness of global pharmacovigilance environment.

If you would like to discuss this role in greater detail or your application / suitability to this or further roles, please call me or email me in confidence. If you are not available or suited to this position, please feel free to pass my details on.
We also have a broad variety of other Biometric specific vacancies available in the UK and throughout Europe. Inclusive of SAS programming, Statistical, Clinical programming, Data Management functions, Regulatory Affairs, Clinical Research, QA, Compliance & Validation.
1st IT/Pharma People are acting as an Agency and or Employment Business
For a confidential consultation call Patrizia Micalizio on 0044 (0) 207 255 6665 or email your CV to patrizia.micalizio@1st-pharmapeople.com


- pharmaceutical, cro, drug safety

- South East