Grand Pharmaceutical Group Limited
（高级）医学经理
Skills
2 months ago
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Important information
Contract type:
Permanent
Location:
Wuhan, Hubei, China
Work mode:
Onsite
Published on:
10 September 2026
What they need
该职位来源于猎聘 1.负责临床研究的医学撰写和医学监查工作，包括：撰写临床研究方案、研究者手册、知情同意书、临床总结报告等，进行中心的医学支持、EDC监查等工作；
- 负责与研究者沟通处理包括研究方案及试验过程中与医学相关问题；
- 完成Pre-IND、IND和NDA/BLA中临床部分资料的撰写及审核
协助上级领导完成对于产品开发策略的制定；
专业技能 1. 临床医学或相关专业，硕士及以上学历，3年及以上肿瘤相关的企业工作经验，有临床经验优先；
2 .具有良好的沟通能力、英语听说读写能力
3 .具有独立完成医学撰写和医学监查的工作能力，且负责完成过至少1项海外临床研究方案的撰写或CSR的撰写或医学监查工作；
4 .具有良好的GCP意识，了解国内外关临床法规需求；
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