Description
Pharmacovigilance Officer- Nordics
Drug Safety- Nordics- CRO- Sweden- PV Associate- PSUR- RMP- PSMF- Clinical Development
A fantastic opportunity has become available for a Drug Safety professional to join a Nordic CRO with more than 15 years experience in conducting clinical trials and medical device studies. The company cover all stages of clinical development from phase I to phase IV and they have offices located in Denmark, Finland, Norway and would like the PV Officer to be located in Sweden.
As a Pharmacovigilance Officer you will:
*Maintain PV systems and documents- PSMF
*Maintain and oversee safety data exchange agreements- SDEA, patient support programs, market research programs and investigator initiated studies
*Compile PSURs and other regulatory Pharmacovigilance/Medical Device documents
*Contribute to Risk Management Plans and collect and track information
*Support safety awareness training
*Support management in literature and health authority safety reports including medical follow-up key interface functions within Regulatory and Quality
An ideal Pharmacovigilance Officer will have:
*Previous Drug Safety/Pharmacovigilance experience
*Life Sciences Degree- preferably MSc or PhD
*English language skills
*Case processing/data handling experience
This is a fantastic opportunity for a junior Drug Safety professional to make the next step up in their career with a CRO who works with a full range of companies including small start-ups to multi-national corporations.
If you are interested in this opportunity and wish to discuss further details about the role or other Drug Safety and Pharmacovigilance positions in the UK and Europe, please contact Sabrina Deo at +44 (0)121 616 3471.
Drug safety, pharmacovigilance, PV, Nordics, Denmark, Sweden, Finland, Norway, CRO, case processing, regulatory, quality, SDEA, Medical Device, RMP, PSUR, Risk Management, data handling, Europe, safety, health authorities
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