relevant to PV or pharmacoepidemiology. Extensive experience of PV in the Pharmaceutical Industry, with focus aggregate report writing and risk management. Experience of orphan drug/rare diseases/biologics preferred safety preferred. Experience in clinical research and/or PV is preferred. Experience with leading or supporting agency inquiries, and product quality issues. Experience in reviewing different aggregate report types Safety reports, and RMPs is mandatory. Prior experience in supporting business development activities
relevant to PV or pharmacoepidemiology. Extensive experience of PV in the Pharmaceutical Industry, with focus aggregate report writing and risk management. Experience of orphan drug/rare diseases/biologics preferred safety preferred. Experience in clinical research and/or PV is preferred. Experience with leading or supporting agency inquiries, and product quality issues. Experience in reviewing different aggregate report types Safety reports, and RMPs is mandatory. Prior experience in supporting business development activities