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. Create, implement and execute procedures to build and maintain database set-up for paper based and/or web based (EDC) clinical data management systems (CDMS) in standard format or CDISC compliant format as required, including the annotation of CRFs

Compliance supervisor

GlaxoSmithKline Pte Ltd
China Jiangsu
2-5 years

Job Description : Site Name: Suzhou Plant Tech Industry Park Posted Date: Oct 15 2021 教育程度/验 大学本科或以上学习,制或化学等相关专业。 至少5年生产业质工作验,熟悉GMP管。 特别知识 熟悉制行业法律法规求,现行GMP标准以制工业标准。 全掌并熟练应用现行GMP知识和质工具(如统计分等)。 技能 具备高度的责任心和主观能动性,并拥有良好人际关系,以出色的沟通能力和解决问

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