- Perform site selection, initiation, monitoring and close-out visits in accordance with the scope of work, Protocol, ICH good clinical practice and applicable local laws
- Preparation of monitoring visit reports as per the SOPs of the Sponsor / company
- Prompt follow up with sites for closure of actionable items
- Provide training to the sites on protocol and study manuals
- Provide clarification to the site team on any doubts/questions on study procedures
- Effective Communication with the investigational site team, Sponsor and regional project lead
- Preparation/review of Ethics committee submission dossiers
- Follow up with the sites for Ethics committee approval and finalization of site initiation date
- Review of supplies at site
- Follow up for recruitment

- Bachelor'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