1. Direct interactions with KFDA
2. KFDA meeting planning, preparation, and presentation
3. Dispute resolution
4. Pre-meeting briefing packages
5. Post-meeting issue analysis and responses
6. Act as direct agents for the sponsor with KFDA
7. SAE reporting and PSUR submissions
8. If required, approval of investigator packets required for release of investigational product
9. If required, develop/review informed consent forms
경력 및 자격요건
1. BS in Pharmacy
2. Preferred over 1 ~ 2 Experienced RA
3. Obtained more than 3 times KFDA Approval in global clinical trial studies
4. Outstanding verbal/written communication skills in English and Korean
5. Ability to manage multiple projects
기타
- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자
담당업무
입사지원
돌아가기
02-6281-
ymlee@nterway.com
