•Responsible for clinical trials that are conducted in Korea
•Management R&D clinical trials and PMSs that are outsourced to CRO
•Oversight and communication with investigative sites, CRO and global study team
•Regulatory documentation and verification
•Development of a good working knowledge of relevant protocol and disease, and FDA, ICH/GCP requirements and relevant regulatory requirement
•Responsible for CRO training
경력 및 자격요건
•Bachelor of Science, Nursing or Pharmacy or masters/PhD in a scientific discipline.
•3~7 years CRA experience including site monitoring
•Knowledge of clinical(ICH-GCP), regulatory and drug development cycle.
기타
- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자
담당업무
입사지원
돌아가기
02-6281-5015
yhw@nterway.com
