出海雷达

合同统计程序员

Contract Statistical Programmer

开发工程限定地区(需当地身份)
公司Iovance Biotherapeutics
薪资未公开
工作地点Australia, Canada, Germany, Netherlands, United Kingdom, United States
地域资格限定地区(需当地身份)
时区要求日间重叠约 9 小时,基本正常作息
用工类型Contractor
发布时间17 天前
数据来源Himalayas
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注意地域限制:该职位明确限定在 Australia、Canada、Germany、Netherlands、United Kingdom、United States 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。

Iovance Biotherapeutics 致力于成为全球在创新、开发和提供肿瘤浸润淋巴细胞(TIL)疗法治疗癌症患者方面的领导者。我们通过利用人体免疫系统识别和攻击每位患者中多种癌细胞的能力,正在开创一种变革性的癌症治疗方法。Iovance 的 TIL 平台已在多种实体瘤中展现出有希望的临床数据。我们致力于细胞疗法的持续创新,包括基因编辑细胞疗法,这可能为癌症患者提供有前景的治疗选择。

简介
Iovance 正在寻找一名合同统计程序员,通过开发、验证和维护临床研究和监管提交的统计编程交付物,支持临床开发项目。该职位将与统计学家、数据管理和其他跨职能团队密切合作,确保在符合 GxP 要求的环境中高质量且及时地交付数据集、表格、列表和图表。理想的候选人具备强大的编程技能,并拥有坚实的统计学或定量科学基础,能够在协作、快节奏的生物科技环境中茁壮成长。

核心职责与任务

  • 根据 CDISC 标准,开发、验证和维护用于创建 SDTM、ADaM 数据集和 TLF 的 SAS 和/或 R 程序。
  • 支持定期安全报告、出版物、会议演讲、IDMC/DSMB 审查、临床研究报告(CSRs)、监管提交、卫生当局请求及其他临时分析和报告需求的统计分析。
  • 确保所有编程活动符合 FDA 21 CFR 第 11 部分、GxP 和内部 SOP。
  • 与生物统计学家、数据管理人员和临床团队合作,定义分析规范并解决数据问题。
  • 对统计程序和输出进行质量控制和详细审查。
  • 开发和维护可重复使用的宏、模板和自动化工具,以提高编程效率。
  • 参与新兴技术和现代编程方法的评估与实施,包括基于人工智能的工具和代理,以增强统计编程流程。
  • 参与编程数据规范的开发和审查。
  • 维护清晰、详尽的文档,以支持审计准备和监管检查。
  • 必须遵守 Iovance Biotherapeutics 的核心价值观、政策和实践。
查看英文原文

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer.
Overview
Iovance is seeking a Contract Statistical Programmer to support clinical development programs by developing, validating, and maintaining statistical programming deliverables for clinical studies and regulatory submissions. This role will work closely with statisticians, data management, and other cross-functional teams to ensure high-quality and timely delivery of datasets, tables, listings, and figures in a GxP-compliant environment. The ideal candidate combines strong programming expertise with a solid foundation in statistics or quantitative sciences and thrives in a collaborative, fast-paced biotech setting.
Essential Functions and Responsibilities

  • Develop, validate, and maintain SAS and/or R programs for the creation of SDTM, ADaM datasets, and TLFs in accordance with CDISC standards.
  • Support statistical analyses for periodic safety reports, publications, conference presentations, IDMC/DSMB reviews, clinical study reports (CSRs), regulatory submissions, health authority requests and other ad hoc analyses and reporting needs.
  • Ensure all programming activities comply with FDA 21 CFR Part 11, GxP, and internal SOPs.
  • Collaborate with biostatisticians, data managers, and clinical teams to define analysis specifications and resolve data issues.
  • Perform quality control and detailed review of statistical programs and outputs.
  • Develop and maintain reusable macros, templates, and automation tools to improve programming efficiency.
  • Contribute to the evaluation and implementation of emerging technologies and modern programming approaches, including AI-based tools and agents, to enhance statistical programming workflows.
  • Participate in development and review programming data specifications.
  • Maintain clear, thorough documentation to support audit readiness and regulatory inspection.
  • Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics.
  • Perform miscellaneous duties as assigned.

Required Education, Skills, and Knowledge

  • Master’s degree in mathematics, statistics, computer science, biostatistics, data science or a related quantitative field with 5+ years of relevant industry experience; or bachelor’s degree in mathematics, statistics, computer science, biostatistics, data science or a related quantitative field with 8+ years of relevant industry experience
  • Strong proficiency in SAS and/or R for clinical trial data analysis and reporting.
  • Working knowledge of CDISC standards (SDTM, ADaM, Define-XML) and regulatory submission requirements.
  • Experience producing TLFs and SDTM/analysis datasets in a pharmaceutical, biotechnology, or CRO setting.
  • Experience with oncology clinical trials or cell/gene therapy programs.
  • Strong analytical, problem-solving, and communication skills.
  • Familiarity with regulatory guidelines (FDA, ICH) and GxP-compliant programming practices.
  • Excellent attention to detail, problem-solving skills, and the ability to manage multiple priorities independently in a remote environment.

Preferred Education, Skills, and Knowledge

  • Master’s degree in mathematics, statistics, or computer science is strongly preferred.
  • Hands-on experience developing AI agents or applying AI/ML-based automation tools to streamline data analysis, programming workflows, or reporting processes is a significant plus.
  • Experience supporting regulatory submissions (NDA, BLA, MAA, or equivalent)
  • Familiarity with electronic submission standards (eCTD) and health authority interactions.

Physical Demands and Activities Required
The physical demands described here represent those an employee may encounter while performing the essential functions of this job. Reasonable accommodation may be provided to enable individuals to perform these functions.

  • Ability to remain in a stationary position for extended periods
  • Ability to move about within an office or remote workspace and exert up to 10 pounds of force occasionally
  • Visual acuity sufficient for preparing and analyzing data, viewing computer screens, and extensive reading
  • Repetitive motion involving wrists, hands, and/or fingers
  • Ability to communicate effectively to exchange information
  • Cognitive: Ability to engage in analytical, conceptual, and problem‑solving activities in a dynamic business environment

Work Environment
This role operates in a professional office or remote work environment and requires routine use of standard office equipment and technology. Employees working remotely are expected to maintain a safe workspace free from recognized hazards.

The annual base salary we reasonably expect to pay is listed. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of the role, job duties/requirements, and relevant education, experience and skills.

Pay Transparency

$70—$80 USD

The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Management retains the discretion to add or to change the duties of the position at any time.

Iovance is committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, our employees and applicants will be considered without regard to an individual’s race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law. If you need assistance or accommodation to apply to one of our opportunities, please contact .

By voluntarily providing information and clicking “Submit Application”, you explicitly consent to the collection and use of your personal information for the purposes described above and in our Candidate Privacy Notice.

Originally posted on Himalayas

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