远程工作雷达

高级/资深统计学家

Senior/Principal Statistician

AI限定地区(需当地身份)日间重叠约 2 小时,需偶尔早起或晚睡
公司Veramed
薪资未公开
工作地点Spain、United Kingdom
地域资格限定地区(需当地身份)
时区要求日间重叠约 2 小时,需偶尔早起或晚睡
用工类型permanent
发布时间2026-08-06
数据来源4dayweek.io
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注意地域限制:该职位明确限定在 Spain、United Kingdom 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。
作息提示:日间重叠约 2 小时,需偶尔早起或晚睡。

Veramed 以两个关键领域为傲:为客户提供最高质量的统计和编程咨询服务,以及为员工提供行业领先的办公环境,包括出色的支持、培训和职业发展机会。我们正在寻找一位高级至首席级别的统计学家加入我们,从事全职工作。我们提供灵活的工作方式(居家、混合或办公室),结构化的培训和发展,以及具有竞争力的薪酬包。

#### 职位描述

该职位的目的是为我们的一个关键FSP客户提供建设性的统计支持。作为高级或首席统计学家,您可能还需要承担监督职责,包括直线管理和/或项目领导,具体取决于经验和兴趣。该职位适合在临床研究和监管提交方面有丰富经验的人士,能够直接与客户合作——包括在没有内部统计支持的情况下。您将能够自信地独立工作,管理自己的工作量,并在多个项目和客户之间做出贡献。良好的沟通能力至关重要,包括向非统计人员解释统计概念的能力,以及向客户团队清晰而自信地进行展示。

#### 主要职责

- 研究层面的统计监督
- 在临床研究中提供项目层面的统计输入
- 审核和监督来自其他CRO的统计交付物
- 开发和/或审核研究文档,包括协议中的统计部分和统计分析计划(SAPs)
- 研究设计活动,包括样本量计算、临时和探索性分析
- 根据需要为客户提供项目的额外统计支持
- 熟练使用R、SAS或其他非SAS语言进行编程(或愿意学习)

#### 经验与技能

**必要条件:**

- 在临床研究环境中拥有高级至首席级别的统计经验
- 在临床研究和监管提交方面有经验
- 能够独立与客户合作,通常没有内部统计支持
- 良好的沟通能力,能够向非统计人员解释统计概念
- 好奇心强,积极主动,有持续学习和提升的动力

**优先考虑:**

- 研究设计和样本量计算经验
- 监管经验
- 对统计学的基本理解或学习意愿

查看英文原文

Veramed prides itself on two key areas: providing the highest quality statistical and programming consultancy to our clients, and offering our employees an industry‑leading working environment with outstanding support, training, and opportunities for career growth. We have an exciting opportunity for a Senior to Principal level Statistician to join us on a permanent basis. We offer flexible working (home, hybrid or office‑based), structured training and development, and a competitive package.

#### The Role

The purpose of this role is to provide high‑quality statistical support to one of our key FSP clients. As a Senior or Principal Statistician, you may also take on a supervisory role, including line management and/or project leadership, depending on experience and interest.This role is well‑suited to someone with significant experience in clinical studies and regulatory submissions, who is comfortable working directly with clients - including situations where there is no internal statistical support. You will be confident working independently, managing your own workload, and contributing across multiple projects and clients. Strong communication skills are essential, including the ability to explain statistical concepts to non‑statisticians and to present clearly and confidently to client teams.

#### Key Responsibilities

- Statistical oversight at study level
- Providing project‑level statistical input across clinical studies
- Review and oversight of statistical deliverables from other CROs
- Development and/or review of study documentation, including statistical sections of protocols and Statistical Analysis Plans (SAPs)
- Study design activities, including sample size calculations, ad‑hoc and exploratory analyses
- Additional statistical support as required across client projects
- Confident coding in R, SAS, or other non‑SAS languages (or a willingness to learn)

#### Experience & Skills

**Essential:**

- Senior to Principal level experience in statistics within a clinical research environment
- Experience working on clinical studies and regulatory submissions
- Comfortable working independently with clients, often without in‑house statistical support
- Strong communication skills and the ability to explain statistical concepts to non‑statisticians
- Curious, proactive, and motivated to continuously learn and improve

**Desirable:**

- Study design and sample size experience
- Regulatory experience
- A basic understanding or willingness to learn Bayesian methods and causal inference modelling
- Experience within Oncology and/or CNS therapeutic areas

#### Opportunities at Veramed

- Presenting at conferences and authoring publications
- Developing and implementing innovative statistical methodologies, study designs, and efficiency‑optimisation ideas
- Line management and peer mentoring opportunities
- Contributing to business process improvements and internal training
- Supporting initiatives linked to employees, the environment, and local communities as part of our B Corp accreditation

#### What to Expect

- A warm, friendly working environment where you can thrive both personally and professionally
- Supportive, open‑door management that actively encourages development
- Exposure to a wide variety of clients and projects, including collaboration with leading global pharmaceutical companies
- The opportunity to work with a truly unique CRO that does things differently — valuing people, relationships, and quality
- The chance to genuinely own your role and shape your career path

If you’re independent, curious, and ready to make a meaningful impact within a forward‑thinking organisation, we’d love to hear from you.

**_Veramed is a B Corp_** _accredited company which means that we use the power of business to build a more inclusive and sustainable economy meeting the highest verified standards of social and environmental performance, transparency, and accountability._

_As an organisation that has people at the heart of it, Veramed is committed to creating a diverse environment and is proud to be an equal opportunities employer. We foster a working culture where employees have integrity, honesty and respect for one another without regard to race, national origin, religion, gender identity or expression, sexual orientation or disability. All qualified applicants will receive equal consideration for employment._

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