Gcp Inspector
CurrentConduct GCP (Good Clinical Practice) inspections in clinical trials across all phases of development in investigator sites, sponsors and CROs (Clinical Research Organizations) and deliver reports on both National (EOF) and European (EMA) competent Authorities as a leading/reporting/contributing inspector. Execute triggered and routine GCP inspections.Expert member of the GCP IWG (EU Inspectors Working Group) in EMA focusing on harmonisation and co-ordination of GCP related… Show more Conduct GCP (Good Clinical Practice) inspections in clinical trials across all phases of development in investigator sites, sponsors and CROs (Clinical Research Organizations) and deliver reports on both National (EOF) and European (EMA) competent Authorities as a leading/reporting/contributing inspector. Execute triggered and routine GCP inspections.Expert member of the GCP IWG (EU Inspectors Working Group) in EMA focusing on harmonisation and co-ordination of GCP related activities at EU level. Member of the IWG subgroup for IWG on future-proofing of GCP inspections. Show less