[Novotech] Pharmacovigilance Associate °æ·Â Á¤±ÔÁ÷ ä¿ë
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[±Ù¹«ºÎ¼ ¹× Á÷±Þ/Á÷Ã¥] • Support to set up the related system and safety database such as Oracle Argus Safety, ArisGlobal ARISg, Veeva VaultSafety, CRScube cubeSAFETY. • Support to set up and update the related SOPs and ensure the regulatory compliance. • Support the PV related work in the clinical projects including but not limited to case processing, review of annual safety report, expedite/periodic reporting of safety information to regulatory authorities/investigators/IRBs/sponsors, and the preparation of safety management plan. • Support to perform post-marketing PV service tasks including but not limited to case handling, literature searching and reviewing, expedited / periodic reporting of safety information to regulatory authorities/sponsors in compliance with regulatory timelines. • Support to prepare periodic aggregate reports (PSUR/PBRER/DSUR) and Risk Management Plan. |
[ÀÚ°Ý¿ä°Ç] • Bachelor of pharmacy/nursing/medicine/biology or a related major. A master/PhD degree is preferred. • 1 year or above Clinical /PV relevant experience is preferred for PV Associate/Specialist; and 2.5 years or above PV relevant experience is preferred for senior PV Associate/Specialist. • Proficient knowledge of safety data base (such as Oracle Argus Safety, ArisGlobal ARISg, Veeva VaultSafety, CRScube cubeSAFETY) are preferred. • Fluent in both written and oral English |
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