- Responsible for all the project deliverables of Clinical Trials
- Assign, train and manage resources
- Manage study budgets
- Ensure compliance in terms of ICH-GCP, Protocol, and other applicable regulations
- Follow up with KFDA. Past Experience in preparation of regulatory dossier and getting trial approval from KFDA will be viewed very positively
- Co-monitoring with CRAs

- Masters's degree in a healthcare or other scientific discipline or equivalent educational qualification
- Additional management qualification / advanced course / degree in Clinical trials is an added advantage
- Strong verbal and written English communication
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint, MS Project and outlook
- Excellent organizational and problem-solving skills
- Effective time management skills
- Ability to manage competing priorities

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