[ 글로벌 제약사 ] Clinical Quality Associate Director
페이지 정보
등록자 :
노정선 Jessie Roh 상무
등록일 : 24-09-11
기본정보
| [ 글로벌 제약사 ] Clinical Quality Associate Director | |||
| 임상ㆍPV | 부장~부장 | ||
상세정보
본문[업무내용] Country QMP creation/maintenance Country quality meetings ASV risk assessment ASVs Quarterly regional quality meetings Training compliance Country QMS review Monitoring Visit Report Compliance Review Study Quality Review Approval Oversight [자격요건] 1. 외국계 제약사 임상파트 경력 2. Quality experience preferred (PM 경력자도 지원 가능) 3. Clinical Research or Quality at least (minimum)10+ years / Project manager / audit, inspection involve experience [근무지] 서울 |
담당컨설턴트
| 노정선 Jessie Roh 상무 | 02-6403-0502 | ||
| jessie@future-cons.com |