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In collaboration with the Medical Director, supports the development of study protocol and amendments, clinical sections of regulatory documents, including investigator brochures, annual safety update reports; contributes to study documents, including AE section of ICF templates, eCRFs and SAE report forms.
Actively manage one or more early or late stage global drug development project teams, executing the program strategy for the specific project, according to the TPP.
直接对接亿级企业家,拓展国内头部民族品牌
知名大型能源领域公司,寻求IT知名大型能源领域公司,寻求IT 总监一名
知名金融公司,寻求IT总监一名
功能性食品开放创新
负责集团的商业智能团队搭建与管理,协助管理层规划,通过数据的方式更好支持业务的可持续发展。