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¿Ü±¹°è CRO»ç-Senior Clincial Research Associate
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¿Ü±¹°è CRO»ç-Senior Clincial Research Associate
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.Responsible to support project team(s) on all project-related issues to ensure all activities are conducted in highest quality standards, in compliance with ICH E6 GCP, local GCP and applicable local regulatory requirements as well as to meet/exceed sponsor''''s expectation, under the supervision of project manager(s)
.Support to develop, compile and/or review all study-related regulatory and administrative documents from investigational sites, monitoring visit reports, work progression reports and other study-required documents
.Support to develop, compile and/or submit dossiers to regulatory and/or ethics committee for review and follow up until approval, if required
.Support in planning, coordinating, organizing and attending all study-related meetings and activities for sites as required
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"1. To support project management, clinical monitoring and/or regulatory affairs operations in all aspects of the project(s)
2. To support study start up activities to ensure swiftest start up and initiation of the study as possible
3. To assist project team(s) in project administrative tasks including statys and finance tracking
4. To support Project Manager and Project Team as Project Assistant as required
Support in operations and/or business''''s continuality by undertaking tasks such as:
1.Support in set up and maintanance of new/existing projects in CTMS as required
2. Provide relevant support and assistance whenever required by the Company and department"
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1. À̷¼ Á¦Ãâó: À̸ÞÀÏ npc@nowpharm.co.kr, ¼ö½ÅÀÚ ÃÖ³«¿ì
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8) ³ª¿ìÆÊ ÄÁ¼³Æà ÁÖ¼Ò : ¼¿ï °³²±¸ »ï¼º·Î508 LGÆ®À©ºô2Â÷ 1412È£
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