生物统计学家
Biostatistician
职位名称：生物统计学家
职位类型：承包商
工作地点：远程
micro1 正在招募生物统计学家，为客户的 AI 基准测试高级项目做出贡献。在此职位中，您将运用专业知识帮助训练下一代 AI 系统。您的工作将影响模型如何学习、推理和执行，通过高质量的真实世界输入。无需 AI 领域经验——您的专业领域知识才是关键。
工作范围
- 设计并撰写专家级评估任务，模拟真实世界的生物统计学挑战，例如临床试验分析、监管提交审查和观察性研究评估。
- 获取、构建和整理真实数据集，包括试验数据、患者记录和方案文件，用于任务使用。
- 为每个评估场景定义正确的方法论解决方案和可辩护的临床解释。
- 开发全面的、包含 35 项以上的评分标准，以方法严谨性和临床推理为依据评估 AI 代理的表现。
- 确保所有任务反映真实世界生物统计学实践的复杂性和深度，避免简化或教科书式的例子。
- 与项目相关方合作，确保交付成果符合监管和科学标准。
优先资格
- 生物统计学、统计学或流行病学硕士或博士学历。
- 在制药、合同研究、医院或学术医疗环境中拥有 4 年以上经验。
- 在临床研究设计、监管文件和观察性研究方法方面有扎实掌握。
- 在真实临床或流行病学数据集上熟练使用 R、Python、SAS 或 Stata。
- 对方法论细节、临床解释和监管敏感性有高度关注。
- 有为监管机构（如 FDA、EMA）准备提交材料的经验者优先。
- 优秀的书面沟通能力，能够撰写详细的评分标准和技术文档。
薪酬结构
薪酬基于产出；专家根据符合项目要求的任务获得报酬。完成工作所需时间可能因专家的经验和工作流程而异。有最低提交要求。专家每周必须提交至少一定数量的任务。
开始时间表与可用性
我们通常在 48 小时内填补职位，正在寻找可以立即投入工作的专家。如果被选中，我们期望您在入职后尽快开始第一项任务。
查看英文原文
Role Title: Biostatistician
Role Type: Contractor
Location: Remote
micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI benchmarking. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.
Scope of Work
- Design and author expert-level evaluation tasks simulating real-world biostatistics challenges, such as clinical trial analysis, regulatory submission reviews, and observational study assessments.
- Source, construct, and curate authentic datasets including trial data, patient records, and protocol documents for task use.
- Define correct methodological solutions and defensible clinical interpretations for each evaluation scenario.
- Develop comprehensive, 35+ item rubrics to evaluate AI agent performance with respect to methodological rigor and clinical reasoning.
- Ensure all tasks reflect the complexity and depth of real-world biostatistics practice, avoiding simplified or textbook-style examples.
- Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific standards.
Preferred Qualifications
- MS or PhD in biostatistics, statistics, or epidemiology.
- 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts.
- Demonstrated command of clinical study design, regulatory documentation, and observational research methodologies.
- Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets.
- Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.
- Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a plus.
- Excellent written communication skills and ability to author detailed grading rubrics and technical documentation.
Compensation Structure
Compensation is output-based; experts are paid per task that meets the project specifications. The time required to complete work may vary depending on the expert’s experience and workflow. Minimum submission requirements apply. Experts must submit a minimum of tasks per week.
Start Timeline & Availability
We typically fill roles within 48 hours and are looking for experts ready to jump in right away. If selected, we expect you to start your first tasks within 24–48 hours of completing onboarding.
Originally posted on Himalayas