1. CRA(임상시험 담당)

∙ BS degree (Major in medicine, pharmacology, veterinary science, nursing)
∙ More than 5-year experience in clinical research at the pharmaceutical industry in Korea
∙ English skill (written & spoken)
∙ A great store of knowledge of ICH guideline and GCP
- Excellent in collaboration and presents good team player
- Having punctuality on pursuing projects

2. RA(제약 허가등록 책임자)

∙ BS/MS/PhD (Major in pharmacology, pharmaceuticals, veterinary, nursing)
∙ More than 7-year experience in regulatory affair at the pharmaceutical industry in Korea
(over assistant manager level)
∙ Have a smooth communication on the job in English (and Japanese, preferably)
∙ Enough experience and knowledge of IND, NDA/aNDA process in Korea
- Understand the trend of ICH & CTD
Trace the current regulatory trends in Korea (regulatory systems, laws, notifications, etc.)
Manage the regulatory consultants and/or CROs appropriately
Preferably, has some connection with KFDA officers

[제출서류] 이력서, 자기소개서

[제출방법] 이메일 접수 shson@iesfkorea.com

[접수기간] : <?XML:NAMESPACE PREFIX = ST1 />2010. 8. 26까지

[연락처] : 02-3439-5023 / 010-7288-2143