pharmacoepidemiology. Experience in clinical research and/or PV is preferred. Experience with leading or supporting agency enquiries and product quality issues. Experience in reviewing different aggregate report types Annual Safety reports and RMPs is mandatory. Prior experience in supporting business development activities meetings. Previous experience with authoring/reviewing PV procedures is preferred. Experience with PV processes timelines and changing priorities. Extensive experience in PV in the Pharmaceutical Industry, with a
pharmacoepidemiology. Experience in clinical research and/or PV is preferred. Experience with leading or supporting agency enquiries and product quality issues. Experience in reviewing different aggregate report types Annual Safety reports and RMPs is mandatory. Prior experience in supporting business development activities meetings. Previous experience with authoring/reviewing PV procedures is preferred. Experience with PV processes timelines and changing priorities. Extensive experience in PV in the Pharmaceutical Industry, with a