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It will involve quality control review of study related documents, study monitoring as it relates to cruelty free studies as well as the creation/revision/review of standard operating procedure SOPs, timely completion of deviations and investigations, and implementation and periodic review to ensure compliance to applicable FDA/health authority regulations and ICH (International Council for Harmonisation), Good Clinical Practice (GCP) guidelines and SOPs.
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知名医疗健康基金招早期项目孵化岗位
外资资管公司招募投资岗位Director/ED/MD (医疗健康)
我们的客户是一家在创新药领域具有卓越声誉和实力的全球企业,致力于研发、生产和销售创新药物,为全球患者提供安全、有效的治疗方案。为进一步扩大中国市场影响力,提升业务规模,现诚邀有志之士加盟,共同开创美好未来。
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