
葛兰素史克
Clinical Program Lead, Oncology
Clinical Program Lead, Oncology
发布于 大约 14 小时前普通员工/个人贡献者
上海市 / 北京市
高级经验
全职员工
仅现场办公
博士
医疗、制药与临床研究
Cross-Functional Collaboration
Strategic Planning
Regulatory Affairs
Matrix Leadership
AI 估算 · 40k–60k
肿瘤临床项目负责人,要求博士学历及多年经验,薪资竞争力强,符合外企高级岗位水平。
职位详情
关于这个职位
作为肿瘤领域临床项目负责人,您将主导中国区临床开发策略的制定与执行,确保临床试验设计与注册合规,并推动创新药物上市
您需要整合内外部资源,领导跨职能团队,以科学和战略视角把控项目风险与质量
最低要求
MD, PhD or PharmD degree with 8-10 years of experience in clinical development/medical practice and/or scientific research in the relevant field.
At least 10 -12 years of experience in Pharmaceutical industry, a track record of success in leading clinical development in China and Global
Excellent knowledge of GCP and regulatory requirements
Strong experience in trial design, planning, operationalisation, reporting and publication
Understanding of clinical research methodology to facilitate innovative trial design and clinical plans with credible data-driven decision making
Experience in inductive and deductive reasoning, and providing mechanisms to interpret and analyse complex information
Relevant expertise in the disease area including biology, potential therapeutic targets, treatment pathways, unmet need and evolving practice
Demonstrated ability to incorporate global aspects into strategic and operational decisions
Proven ability of strategic thinking, practical problem solving, multidisciplinary collaboration and agile decision making
Experience in line management /matrix leadership
Proven ability to communicate effectively with credibility, accuracy, and confidence with internal and external stakeholders
Proficiency in English
工作职责
Provide clinical leadership and asset/disease expertise for the clinical trial program and indications in scope
Provide scientific and strategic input to China component of IEP for the program
Provide matrix leadership at program level to ensure integrated approach, robust planning and execution oversight; may lead TMT/IET
Deliver robust trial design, protocols, study reports and appropriate data interpretation required for local registration, PAC and other Ph4 studies through collaboration on TMT
Responsible for timely assessment and mitigation of risks associated with clinical trial and scientific content delivery at program level
Responsible for medical governance for the clinical program in scope
Clinical lead for the program for external collaborators, regulatory agencies and GSK Global, as appropriate.
Responsible for making recommendations to TAL/IET Leader and senior stakeholders on benefit risk assessment, Go/No-go criteria, and Clinical PoS for the program in scope
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葛兰素史克 的其他在招职位
(Senior Executive/Executive/Senior)Medical Representative/(执行/专员/高级)医药代表
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