流行病学与方法创新总监
Director, Epidemiology & Methodological Innovation
对精准医疗和推动医疗行业发展充满热情吗?
底层技术的最新进展终于使人工智能能够以有意义的方式影响临床护理。Tempus 的专有平台连接整个现实世界证据生态系统,为医生提供实时、可操作的见解,提供关于在正确时间给正确患者正确治疗的关键信息。
流行病学与方法创新总监将为 Tempus 的生物制药合作伙伴开展高影响力的研究,处于传统结果研究和尖端数据科学的交汇点。这是 Data Business 中一个高可见度、面向客户的职位。你不仅会应用现有的框架;你还将开发和验证新颖的流行病学方法,以释放 Tempus 多模态数据集的全部潜力。理想的候选人是一位科学愿景家,能够将复杂的非线性数据转化为符合监管标准的见解,加速药物研发并改善患者预后。
主要职责
- 方法创新:领导针对真实世界证据(RWE)的新方法开发,包括使用外部对照组(ECA)、高维数据中的因果推断,以及纵向临床数据与分子/基因组特征的整合。
- 研究设计与实施:负责回顾性数据库分析的全流程执行。你将成为研究方案的主要架构师,确保它们突破当前健康经济与结果研究(HEOR/RWE)的标准,同时保持科学严谨性。
- 科学思想领导力:作为生物制药客户的主题专家,为其提供“首创”研究设计的建议。你应通过高质量的论文发表和在 ISPOR、ISPE 和 ASCO 等会议上的演讲,为更广泛的科学界做出贡献。
- 客户战略与合作:与关键客户经理和业务发展团队合作,识别可以利用新方法解决“无法解决”客户问题的机会(例如罕见疾病表征或复杂生物标志物验证)。
- 跨职能协同:在数据科学、生物统计学和产品团队之间架起桥梁,将成功的创新方法产品化,确保它们在 Tempus 生态系统中可扩展。
- 项目管理与质量:确保所有创新研究符合严格的监管和伦理标准(如 GEP、HIPAA),并符合相关法规要求。
查看英文原文
Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
The Director of Epidemiology & Methodological Innovation will lead high-impact research for Tempus’s biopharma partners, sitting at the intersection of traditional outcomes research and cutting-edge data science. This is a high-visibility, client-facing role within the Data Business. You won’t just apply existing frameworks; you will develop and validate novel epidemiological methods to unlock the full potential of Tempus’s multimodal datasets. The ideal candidate is a scientific visionary who can translate complex, non-linear data into regulatory-grade insights that accelerate drug development and improve patient outcomes.
Key Responsibilities
- Methodological Innovation: Lead the development of novel approaches for RWE, including the use of external control arms (ECA), causal inference in high-dimensional data, and the integration of longitudinal clinical data with molecular/genomic signatures.
- Research Design & Implementation: Oversee the end-to-end execution of retrospective database analyses. You will act as the primary architect for study protocols, ensuring they push the boundaries of current HEOR/RWE standards while maintaining scientific rigor.
- Scientific Thought Leadership: Serve as a subject matter expert for biopharma clients, advising them on "first-in-kind" study designs. You are expected to contribute to the broader scientific community through high-impact publications and presentations at conferences like ISPOR, ISPE, and ASCO.
- Client Strategy & Partnership: Partner with Key Account Directors and Business Development to identify opportunities where novel methodology can solve "unsolvable" client problems (e.g., rare disease characterization or complex biomarker validation).
- Cross-Functional Synergy: Bridge the gap between Data Science, Biostatistics, and Product teams to productize successful novel methods, ensuring they are scalable across the Tempus ecosystem.
- Project Management & Quality: Ensure all innovative research meets stringent regulatory and ethical standards (e.g., GEP, HIPAA), delivering high-quality results on timelines that match the pace of the biopharma industry.
Qualifications
- Education: PhD (preferred) or PharmD in Epidemiology, Biostatistics, Health Economics, or a related quantitative field.
- Experience: 7+ years in HEOR/RWE, with at least 3 years in a leadership capacity.
- Deep expertise in oncology is required.
- Methodological Mastery: Proven track record of developing or implementing advanced methods (e.g., target trial emulation, propensity score applications in complex cohorts, or machine learning-augmented epidemiology).
- Technical Proficiency: Advanced skills in R or SAS. Experience working with "messy" real-world data (EHR, claims, and/or genomic data) is essential.
- The "Consultant" Mindset: Exceptional ability to walk into a room of biopharma executives and simplify complex methodological hurdles into a clear strategic roadmap.
- Leadership: Demonstrated experience mentoring junior scientists and leading cross-functional squads in a fast-paced, high-growth environment.
CHI: $170,000-$230,000NYC/SF: $180,000-$250,000The expected salary range above is applicable if the role is performed from California and may vary for other locations (Colorado, Illinois, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.
Additionally, for remote roles open to individuals in unincorporated Los Angeles – including remote roles- Tempus reasonably believes that criminal history may have a direct, adverse and negative relationship on the following job duties, potentially resulting in the withdrawal of the conditional offer of employment: engaging positively with customers and other employees; accessing confidential information, including intellectual property, trade secrets, and protected health information; and appropriately handling such information in accordance with legal and ethical standards. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Originally posted on Himalayas