• Responsible for preparing, organizing, managing and monitoring clinical researches. Obtaining and maintaining essential documentation and verifying that the study is being carried out in accordance with local regulations, GCP, internal procedures and the protocol requirements
• Perform site selection, initiation, monitoring and close-out visits
• Responsible for Site management from the study set-up to study completion including IRB related tasks, study payment, study materials and Study Master Files
• Support in planning, coordinating, organizing and attending all study-related meetings and activities for sites as required
• Participate in the preparation of audits and inspections as required
• Ensure data query resolution and accurate and timely reporting of Serious Adverse Events
• Train, support and advice Investigators and site staff in study related matters
• Maintains timely and effective communication among team members, CRO and site staff.
경력 및 자격요건
•Minimum 3 years experiences as CRA
•Good command of English & MS Office
•Good communication
•Work as a team
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
