1. ¸ðÁýºÎ¹®: Associate Clinical Operations Manager
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*Responsible to ensure all designated clinical/site monitoring/projectmanagement activities are conducted in highest standards
-Responsible for performing all monitoring aspects of clinical trials
-Perform site selection, initiation, monitoring and close-out visits
-Develop, compile and/or review all study-related regulatory andadministrative documents from investigational sites, monitoring visit reports,work progression reports and other study-required documents
-Support/assist in feasibility studies, site and investigatoridentification as required
-Resource development/planning/management/ budget management
-Support business development activities and changeorder form for out of scope work/activities negotiation and discussionsinternally and with sponsor as required
ÀÚ°Ý ¿ä°Ç:
- Minimum 7-8 years relevant experience in clinical research
- Minimum 5 years direct experience as monitor in clinical studies
2. ÀüÇü
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- À̸ÞÀÏ Á¦Ãâ: ck_recruit@cmicgroup.com
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