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Focusing on CNS, Neurology and orphan therapeutics area's we are searching for candidates who would be responsible for the direct management of activities related to out clients Pharmacovigilance system, compliance assurance with global Regulatory Health Authorities, and serving as Deputy QPPV.
Other duties will include but not limited to being involved in the support for both commercially marketed and development products, the assessment of emerging safety signals, assessment and recommendations for labeling, and oversight of our clients distributors/vendors to ensure compliance. Candidates will also be involved in management/oversight of risk mitigation measures and supporting PSMF oversight/management and revision.
This is a superb and exciting new project so candidates will need to demonstrate exceptional communication skills as you will be communicating at all levels.
Candidates wishing to apply will need to have a minimun of 5 years direct pharmacovigilance experience, preferably wiht pharmaceuticals and/or biologics and have strong knowledge of PV quality systems and regulatory requirements across the US/Canada and other health authorities.
We are able to offer an exciting and very competitive rate to the chosen candidate.
If this is of interest to you, please contact Kathryn
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