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Salary
≈ $26k – $56k per year (Estimated)
Location
In office (Shanghai)
Seniority
Middle · 3+ years exp

Confirmed on the employer's own hiring board on Nov 9, 2026. First seen by Alion on Mar 17, 2026. Simcere Pharmaceutical scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Simcere Pharmaceutical is a Nanjing-based pharmaceutical group that researches, manufactures and sells innovative and generic drugs in China, with a focus on oncology, neuroscience, autoimmune and infectious diseases. Listed in Hong Kong, it reports ten innovative drugs on the market and more than 45 products on the national reimbursement drug list, including the anti-cancer drug Endu and the anti-stroke drug Sanbexin, and it operates in Nanjing, Shanghai, Beijing, Haikou and Yantai. It hires validation and quality engineers, clinical project managers, medical marketing, sales force effectiveness, data and business development staff, and interns.

工作职责 / Responsibilities

岗位职责

1. 组合管理与战略规划

负责公司肿瘤领域早期至后期临床试验项目的组合管理,建立和维护跨项目的优先级协调机制。

参与制定年度及长期临床开发计划,基于科学逻辑、市场竞争格局和资源约束,为管线项目的“进、退、停”提供决策依据。

识别并管理跨项目间的相互依赖关系,规避潜在冲突,实现协同增效。

2. 项目全生命周期管控

监督核心临床试验项目的关键里程碑(如首例入组、数据库锁定、NDA递交),及时发现并预警重大延误或风险。

推动跨职能团队(医学、运营、注册、统计、数据管理)的高效协作,确保项目执行符合GCP法规、质量标准和时限要求。

主导项目组合层面的预算制定与成本控制,合理调配资金,确保高潜力项目的资源倾斜。

3. 流程优化与体系建设

建立健全针对肿瘤产品线的项目管理体系(PMO),优化SOP、工具模板及决策评审机制。

推动数字化项目管理工具的应用,提升组合层面数据的可视化程度,实现基于大数据的实时决策。

负责项目管理团队的人才梯队建设与能力提升。

4. 对外沟通与合作

支持与潜在合作伙伴(BD项目)的尽职调查,从项目管理角度评估引进项目的可行性与资源匹配。

参与关键意见领袖(KOL)沟通及监管机构(NMPA/FDA)会议的准备,确保项目信息的准确呈现。

任职要求

1. 教育背景

医学、药学、生命科学等相关专业硕士及以上学历,博士优先。

2. 工作经验

3年以上创新药临床研发经验,有肿瘤药物领域经验。

任职要求 / Requirements

任职要求:

1.思路清晰,沟通能力强,能够清晰总结事务进展要点及主要障碍;

2.文书能力强,ppt,word, 邮件的产出清晰明了;

3.责任感强,对项目的推进有责任心。

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