Sr. Stat Programmer
工作标题：高级统计程序员职位位置：孟加拉，卡纳塔克州印度工作地点类型：远程工作合同类型：全日制工作资深级别：工作概述 副总统计程序員在我们的组织中发挥着关键作用，确保数据准确性和统计编程任务的完整性。直接向部门经理报告，这个职位需要高水平的统计编辑专业知识，并要求个人跨多个团队合作以提供高质量及时结果。获胜的候选人将负责监督数据分析项目，辅导初级程序员和实施支持临床试验的编程解决方案。在这个角色中，熟练使用统计软件工具以及对监管要求的强有力的理解是必不可少的。副总统计程序员预计会领导促进我们的流程的举措，为我们研究目标进步做出重大贡献。基本功能 · 领导多项项目的统计计划活动，确保数据完整性和交付产品的准确性 •通过 SAS 编程开发和验证数据集和输出，确保符合 ADM 和 SDTM 模型等 CDISC 标准。•监督并指导年轻统计程序员，提供指导和培训以提高他们的技能和绩效。•与各部门合作，将编程任务与项目时间表和目标相一致，确保及时交付结果。•制定和实施支持临床试验数据分析的编程解决方案，遵守法规要求和 IQVIA 标准。•审查和验证统计编程工作，保持高质量标准和符合内部和外部指南。• 作为数据管理，生物统计学和其他部门之间的联系人，以确保统计编程活动的无整合。•参与战略规划和决策流程，促进编程方法及效率。• 在组织内部制定统计编制最佳实践和标准运营程序。•与客户和组织领导层合作实现根据业务要求共同目标。实现服务卓越性。资格 · 学士学位统计或计算机科学或
查看英文原文
Job Title: Sr. Stat Programmer
Job Location: Bengaluru, Karnataka, India
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Job Overview
The Associate Principal Statistical Programmer plays a crucial role in our organization, ensuring data accuracy and integrity in statistical programming tasks. Reporting directly to the department manager, this position demands high-level expertise in statistical programming and requires the individual to collaborate across multiple teams to deliver high-quality, timely results. The successful candidate will be responsible for overseeing data analysis projects, mentoring junior programmers, and implementing programming solutions that support clinical trials. Proficiency in using statistical software tools and a strong understanding of regulatory requirements are essential in this role. The Associate Principal Statistical Programmer is expected to lead initiatives that enhance our processes, contributing significantly to the advancement of our research objectives.
Essential Functions
- Leads statistical programming activities for multiple projects, ensuring data integrity and accuracy in deliverables
- • Develops and validates datasets and outputs using SAS programming, ensuring compliance with CDISC standards such as ADaM and SDTM models.
- • Oversees and mentors junior statistical programmers, providing guidance and training to enhance their skills and performance.
- • Collaborates across departments to align programming tasks with project timelines and objectives, ensuring timely delivery of results.
- • Develops and implements programming solutions that support clinical trial data analysis, adhering to regulatory requirements and IQVIA standards.
- • Reviews and validates statistical programming work to maintain high quality standards and compliance with internal and external guidelines.
- • Acts as a liaison between data management, biostatistics, and other departments to ensure seamless integration of statistical programming activities.
- • Participates in strategic planning and decision-making processes to advance programming methodologies and efficiencies.
- • Contributes to the development of best practices and standard operating procedures for statistical programming within the organization.
- • Partners with customers and organizational leadership to achieve common objectives as per business requirements. Achieve service excellence.
Qualifications
- Bachelor's Degree Statistics or Computer Science or related field Req
- • Master's Degree Statistics or Computer Science Pref
- • Ability to analyze and interpret financial data The candidate should effectively oversee statistical programming tasks with accuracy and integrity to ensure data-driven decisions.
- • Demonstrated analytical skills Must apply high-level analytical skills to support clinical trials and data analysis projects.
- • Demonstrated problem solving skills Responsibility for implementing programming solutions to resolve complex data issues.
- • Proficient in English written and verbal communication skills Able to clearly communicate programming solutions and mentor junior programmers effectively.
- • Builds and manages effective teams Expected to lead initiatives across multiple teams, enhancing processes and contributing to research advancements.
- • Possesses strong technical aptitude Proficiency in statistical software tools is essential for overseeing data analysis projects.
- • Ability to work within tight timeframes and meet strict deadlines Required to deliver high-quality and timely results while adhering to regulatory requirements.
- • Experience in a regulated environment A strong understanding of regulatory requirements is necessary to support clinical trials.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
This job is curated by Lifelancer.
Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.
Please apply via Lifelancer platform to get connected to the application page and to find similar roles.
Originally posted on Himalayas