1. Lead the regulatory affairs function in Korea
2. Key regulatory interface with the country president
3. Develops and maintains excellent knowledge of regulatory procedures and environment and establishes and maintains a network with the relevant policy makers and regulatory agencies in Korea
4. Accountable for executing regulatory strategies in Korea, their subsequent implementation and ensuring successful registration to commercialize products
5. Facilitate product registration in Korea by implementing appropriate process and systems and working closely with KFDA
6. Accountable for ensuring effective product maintenance and lifecycle managment, in line with legal/regulatory requirements and country business needs
7. Develop and and evaluate regulatory intelligence and maximize opportunities to expedite the registration process in Korea
8. Accountable for implementing process for the review and approval of advertising and promotional materials and events(ZINC Maps)
경력 및 자격요건
1. Graduate in pharmacy
2. About 12~15 years experience in managing regulatory function in the pharmaceutical industry
3. Good and broad knowledge of the drug development process
4. Has good knowledge and experience in managing and conducting local and global clinical trials
5. Exceptional command of English
기타
- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자
담당업무
입사지원
돌아가기
02-6281-5045
cwlim@nterway.com
