우리회사의 자랑거리를 #태그로 표현해보세요 우리 회사에 대해 4줄 이내로 소개해주세요 [Novotech] CRA PASS (PMS/OS) 경력 정규직 채용 노보텍아시아코리아(주) 모집부문 및 자격요건 담당업무 자격요건 인원 Responsibilities: * CRAs primary responsibility is to build relationships with Principal Investigators, study co-ordinators, pharmacists, and all relevant site trial personnel to ensure the efficient, expedited, and smooth management of clinical trials. * In collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start-Up Associate (RSA), prepare site essential documents, and support the ethics and regulatory submission and approval processes as needed. * Ensure recruitment of participants as per the site target. Drive site recruitment and engagement initiatives and prepare site-specific recruitment plan(s) and update as required. * Monitoring of investigational sites as per ICH GCP §5.18 (Monitoring) and the Clinical Monitoring Plan (CMP) for each study. This includes all monitoring visit types across all phases of a clinical trial including Site Selection, Site Initiation, Site Monitoring and Site Close Out, unblinded pharmacy visits, and co-monitoring visits. Visits can be conducted either onsite or remote as per CMP. * Responsible for quality study management and monitoring deliverables at the country and site level; follows project requirements and applicable country rules, with moderate oversight from the LM or PM. * Provide written and verbal site updates (including monitoring visit reports) on study progress to the PM/LCRA according to the study requirements/timelines as documented in the Clinical Monitoring Plan and Sponsor/Novotech SOPs. Escalate all key issues as per Issue Escalation SOP. [근무부서 및 직급/직책] 직급/직책: 사원 Experience and Qualifications * At least 2years of independent clinical monitoring experience * Graduate in a clinical or life sciences-related field. * Relevant experience/qualifications in allied professions may also be considered. * Must have good time management skills, attention to detail, be able to work well in a team, and be computer literate. * Preferably experience of working in the research, pharmaceutical industry or a related field * Strong communication skill both in written and spoken Korean & English * Excellent interpersonal and team collaboration skill with a genuine commitment to contributing to the development of innovative treatment [자격요건] 경력사항: PMS 경력(2년 이상 ) 학력사항: 대학교(4년)졸업 [우대사항] 전공계열: 의/약학계열 1 명 근무조건 고용형태: 정규직(수습기간6개월) 급여조건: 연봉 협의 후 결정 전형단계 및 제출서류 전형단계: 서류전형 >; 폰스크리닝 >; 실무진면접 >; 레퍼런스체크 >; 최종합격 추가 제출서류 영문이력서(MS-Word 또는 PDF) 접수방법 접수방법: 자사 홈페이지 기타 유의사항 입사지원서 및 제출서류에 허위사실이 있을 경우 채용이 취소될 수 있습니다. 00
의료·보건·복지>약사·제약>CRA
