● Job description
Responsible for all regulatory affairs activities, operational project teams
Close collaborating and communication with other internal functional teams
Supervise Project management RA Strategy & Program Timeline Development
Responsible for all national and global RA Agency communications and interactions

● Qualification
Over 10-15 years experience of project management & regulatory affairs
Experience as in strategic leadership of regulatory affairs in major (bio)pharma.
Experience in novel biological entity & biosimilar drug development.
Experience in operational execution of regulatory affairs accelerated programs
Excellent Project Management and communication skills and interaction
Experience of dealing with Regulatory authorities and across functional groups

- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자
- 이력서에 연락처, 희망연봉 기재