[위키씨알오] CRA 경력 모십니다.

모집부문 및 상세내용모집부문상세내용CRA 담당업무WIKICRO CO팀 O명ㆍWrite and edit study documentsㆍStudy set-up including IRB approval, study contractㆍParticipated in the process of identification and selection of investigators in collaboration with PMㆍFacilitate preparation and collection of site level documents, especially ensure all document collected prior to study initiationㆍPrepare and submit IRB amendment and ensure that IRB is updated regarding protocol amendments, SAE(if applicable) etc.ㆍSubmit annual report to IRB as appropriateㆍExecute site initiation and training activitiesㆍUndertake monitoring visit within the correct timeline and ensure with report that all activities such as source data verification are completed according to the monitoring planㆍManage study site and training for site staffㆍEnsure site activities in line with milestones (i.e. Startup, recruitment, closeout, etc.)ㆍManaging trial master file, and ensure investigator file completed as requiredㆍDistribute and maintain all relevant study documentsㆍDistribute and track all clinical trial supplies, e.g. CRFs, investigational product, lab kits and ensure that sites have sufficient supplies to continue the study.ㆍAssure continual GCP, ICH and SOP compliance (Informed consent process, Source data verification, AE and SAE reporting etc.)ㆍWrite report related to clinical study: Initiation report, Monitoring visit report, Note to fileㆍPerform data query resolution processㆍCommunicate with the PM, other CRAs, Sponsor and site staff as appropriateㆍTrack patient recruitment by contacting investigators on a regularly basis for individual sites and discuss potential problems with PMㆍUndertake other project related tasks, as assigned by the PMㆍCommunicate with data management staffs regarding data flow and data query processing maintain awareness of current development in the therapeutic areas relevant to his/her project(s), by reading scientific and medical literatureㆍUndertake non-project related tasks as appropriate as assigned by the PMㆍDevelop collaborative relationships with investigator sitesㆍAssist in a variety of projects as required and perform such other duties as may be assigned자격요건및 우대사항담당업무ㆍ※ 자격요건ㆍ학력 : 대졸 이상 (4년)ㆍ유관경력 3년이상 必※ 우대사항ㆍ협업 및 커뮤니케이션에 자신 있다면 플러스 점수!ㆍ유연하고 창의적인 문제 해결 능력 보유자라면 분이라면 절대 놓치지 않겠습니다.ㆍ팀워크와 소통에 자신 있는 분들 집중! 같이 일할 때 맘 편한 분이라면 저희와 찰떡일 거예요. ㆍ기타 필수 사항 우대사항근무조건ㆍ근무형태:정규직(수습기간)-3개월ㆍ근무일시: 09:00~18:00 ㆍ근무지역:(13558) 경기 성남시 분당구 성남대로331번길 11-15 봉우빌딩 4층 - 수인분당선 정자 에서 200m 이내전형절차 서류전형 1차면접2차면접 최종합격접수기간 및 방법ㆍ접수기간:2026년 06월 25일 ~ 2026년 07월 25일ㆍ접수방법:사람인 입사지원ㆍ이력서양식:사람인 온라인 이력서ㆍ제출서류:이력서유의사항ㆍ학력, 성별, 연령을 보지않는 블라인드 채용입니다. ㆍ입사지원 서류에 허위사실이 발견될 경우, 채용확정 이후라도 채용이 취소될 수 있습니다.ㆍ모집분야별로 마감일이 상이할 수 있으니 유의하시길 바랍니다.