글로벌cro aCOM
페이지 정보
등록자 :
강대필상무
등록일 : 21-02-19 09:30
기본정보
| 글로벌cro aCOM | |||
| 임상 | 과장~팀장 | ||
| 무관 | 무관 | ||
| 서류전형 -> 1차면접 -> 2차면접 | |||
| 2021-02-19 | 채용시 | ||
상세정보
본문[담당업무]
*Responsible to ensure all designated clinical/site monitoring/project management activities are conducted in highest standards -Responsible for performing all monitoring aspects of clinical trials -Perform site selection, initiation, monitoring and close-out visits -Develop, compile and/or review all study-related regulatory and administrative documents from investigational sites, monitoring visit reports, work progression reports and other study-required documents -Support/assist in feasibility studies, site and investigator identification as required -Resource development/planning/management/ budget management -Support business development activities and change order form for out of scope work/activities negotiation and discussions internally and with sponsor as required [자격] -Minimum 7~8 years relevant experience in clinical research -Minimum 5 years direct experience as monitor in clinical studies *People managing 경력 필수는 아니나 경력 있으면 우대 |