【 Job Description】 Responsible for clinical trial data management, including database design, validation, and maintenance Draft and review Data Management Plan (DMP), Edit Check Specification, and other related documents Perform data cleaning, and collaborate with CRA/CRC and biostatistics teams to ensure data accuracy and integrity Handle data import, coding (e.g., medication, AE/SAE coding), and database lock procedures Support the use and maintenance of data management systems (e.g., Medidata Rave, Oracle Clinical) Collaborate with global teams, with strong English communication skills required; Japanese proficiency is a strong plus 【Requirement】 Bachelor’s degree or above in life sciences, pharmacy, biostatistics, public health, or related fields Minimum 2 years of experience in clinical data management (CRO or pharmaceutical industry experience preferred) Familiar with ICH-GCP and clinical data management processes Fluent English communication skills (written and spoken) are required Japanese proficiency is a strong advantage 【 應徵方式 】 - 方法一:投遞此篇104 - 方法二:直接投遞給我們https://reurl.cc/0W43pA *****小提醒*****在介紹自己的部分,告訴我們想看 CDM 的職位 - 方法三:加入官方Line 後輸入 CDM Line: http://lin.ee/gPk8luL Line: @ghchunting
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(經常性薪資達 4 萬元或以上)
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