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PV(pharmacovigilance) |
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- Case processing of solicited adverse event reports (case data entry, MedDRA coding, drafting
initial narratives) including review of related documents and follow-up
- Regulatory reporting of individual case safety report(ICSR)/aggregate reports and other safety issues
- Monitor incoming cases and queries in PV mailbox
- Review medical literature and all source of information to update company knowledge with regards to
drug safety
- Establishing/maintaining SOP¡¯s processes, practice and guidelines
- Outsourced PV works management
- Archiving safety documents |
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- Possess up-to-date knowledge of PV regulations
- Experience in a pharmaceutical or biotechnology company (as a PV or CT staff)
- Bio ÀǾàǰ Çã°¡ °æÇèÀÚ
- Good Command of English
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Nego. |
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~ 12. 8. 19 ±îÁö |
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02-597-1780 |
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[Á¢¼ö¹æ¹ý]E-mail : jiko01@kohuman.com (À̸ÞÀÏ Á¢¼ö¸¸ °¡´É) |
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