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高级统计程序员(客户专属 - 仅限中国)

Senior Statistical Programmer (Client-dedicated - China only)

开发工程明确接受中国求职者
公司Syneos Health India Private Limited
薪资未公开
工作地点China
地域资格明确接受中国求职者
时区要求日间重叠约 9 小时,基本正常作息
用工类型Full Time
发布时间昨天
数据来源Himalayas
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明确接受中国求职者:该职位的地域要求包含中国,可正常投递。

高级统计程序员(客户专属 - 仅限中国)
Syneos Health® 是一家领先的全集成生命科学服务组织,致力于加速客户成功。我们与药物研发和商业化全过程中的创新者合作,帮助他们应对复杂性、预见变化并加快进展。

我们的临床解决方案团队成员以药物开发的思维行事,运用多年的经验和专业知识,真正理解客户需求,并在我们打造的解决方案中代表这些需求。

无论您加入我们作为功能服务提供商合作伙伴,还是全服务环境中的成员,您都将与充满热情的问题解决者合作,作为团队不断创新,帮助我们的客户实现目标。我们敏捷且有动力去交付成果——为彼此、我们的客户,最重要的是,为那些需要帮助的人。

了解您的25,000名未来同事已经知道的内容:
为什么选择 Syneos Health
• 我们热衷于发展员工,通过职业发展和晋升;支持性的直线管理;技术和治疗领域培训;同行认可和全面奖励计划。
• 我们致力于建设一个包容的文化——您可以真实地做自己。这背后的核心是我们“驱动交付”的使命,体现了同事们每天展现的热情,塑造能够显著影响他人生活的解决方案。
• 我们不断打造我们所有人都希望工作的公司,也是客户希望与之合作的公司。为什么?因为我们知道,当我们将来自世界各地的聪明人才聚集在一起时,我们可以塑造医疗健康的未来,为客户带来影响,并定义患者进步的速度。

职位职责

  • 使用 SAS 或其他软件开发定制编程代码,根据统计分析计划和编程规范生成汇总表、数据列表、图表和派生数据集。
  • 确保输出符合质量标准和项目要求。执行验证编程,并与其他程序员、生物统计学家和其他项目团队成员合作解决差异或发现的问题。向项目团队成员通报编程进展和需要他们关注的问题。遵循适用的 SOP、WI 和相关法规指南(如 ICH)。
  • 保持项目文档井然有序、完整且最新。
查看英文原文

Senior Statistical Programmer (Client-dedicated - China only)Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:
Why Syneos Health
• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities

  • Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications.
  • Works to ensure that outputs meet quality standards and project requirements. Performs validation programming and works with other Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings. Keeps project team members informed of programming progress and issues requiring their attention. Follow applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH).
  • Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs ensuring inspection readiness.
  • Manages scheduling and time constraints across multiple projects at a time, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload. Develops specifications for datasets and outputs of any complexity according to statistical and sponsor requirements. Anticipates and addresses potential programming issues, reflects forethought, establishes the basis for efficient programming and accurately defines all variables to be accepted by peer review and sponsor/requestor with little rework.
  • Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others.
  • Conducts effective internal meetings (appropriate in format, frequency and attendance). Distributes relevant information in advance. Ensures minutes are promptly and accurately distributed. Follows action items through to completion, and maintains order and focus of meetings, working toward consensus. Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business. Negotiates and establishes accurate time estimates for completion of study programming activities with internal team members and statistical programming management, and completes project programming activities within timeframe allotted.
  • Acts as the lead statistical programmer. Directs the programming activities of other programming personnel and monitors progress on programming deliverables. Reviews project documentation such as Statistical Analysis Plan, mock shells, programming specifications, annotated CRFs, and SAS database design. Provides feedback to the appropriate project team members which reflects forethought and reduces inefficiencies in programming activities.
  • Participates in sponsor meetings, kickoff meetings, and bid defense meetings as statistical programming representative, as required by sponsor. Contributes to the mentoring of programming personnel through developing training courses, presenting training materials, reviewing work, and providing feedback or guiding new associates in process. Transfers deliverables. Performs other work-related duties as assigned.

Qualifications:

  • Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of degree, an equivalent combination of education and demonstrated programming experience.
  • Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.
  • Excellent written and verbal communication skills.
  • Ability to read, write, speak and understand English.

Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Originally posted on Himalayas

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