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