-IIT & SIT Management
-Site Management & Monitoring
-In-house documentation
-IRB Submission
-Study Set up (Protocol development, Investigators’ Meeting)
-Site contract, Investigators’ fee management
-Other study related operation tasks

-University degree(pre in science or disciplines of health or degree in nursing
(MS degree preferred)
-3 years clinical research experience in a CRC/CRO/Pharmaceutical/Medical device Company with clinical trial monitoring experience
-Strong knowledge of ICH-GCP guidelines and applicable regulatory requirements
-Excellent oral and written communication skills in English
-Good interpersonal skills able to motivate the site staff and implement the study successfully

- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자