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Acts as a primary site contact and site manager for all aspect in support of clinical trial
Site monitoring in accordance with the SOPs, ICH-GCP, and relevant regulations
Track and manage study budget, contract and study medication
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1- 3 years clinical research experience in a CRO or Pharmaceutical Company with experience in monitoring on-site clinical trials
Strong knowledge of ICH-GCP guidelines and applicable regulatory requirements
¿µ¾î communication °¡´ÉÇϽŠºÐ
Good interpersonal skills able to motivate the site staff and implement the study successfully
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À̸ÞÀÏ : kelly1050@naver.com ȤÀº hs@mstone.co.kr
¿¬¶ôó : 010-8911-5018, 02-584-9605
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