1. 모집구분

2. 근무조건

고용 형태 : 계약직

급여 : 연봉 추후 협의

3. 응시자격

4년제 정규대학 졸업 이상인자

해외/국내 의료기기/제약 임상연구 유경험자

영어 능통자 우대

GCP, CRA 교육 등 임상교육 관련 이수증 보유자 – 이력서 접수 시, 이수증 첨부 必

4. 담당업무

IIT&SIT MANAGEMENT

SITE MANAGEMENT & MONITORING

IRB related Activities

Essential document management

Study Start-up including site trainings,etc

Site contract

Investigator’s fee management

Study closure

Regular report to related departments

Other study related operation tasks

5. 업무프로세스

( based on 4 sites of multi-center study)

IRB documentation preparation and submission

IRB Review responding and modification

Contract preparation and modification

Study documents (ISF, CRFs etc )

Investigator’s initiation meeting(includingmeeting material preparation)

Site Trainings

Regular monitoring

Investigator’s study payment: once everyyear-TBD

Regular report to Marketing and HQ CR team: every month (every week if necessary)

SAE/AE/any unexpected report to IRB ifnecessary

Investigator’s follow-up meeting andmeeting material preparation : number of investigator’s follow-up meeting willbe decided

Closure of study : all related activities toterminate the study including IRB, HQ, and investigators’

6. 채용일정

서류접수 : 영문이력서 접수(이메일 접수-heather.kim@limacorporate.com)

서류전형 결과

1차 면접

2차 면접(필요 시)

[출처] [리마 코리아] 의료기기 CRA 채용 (신약 개발임상 연구원 모임) |작성자 yelim1220