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统计程序员-未来职位(印度)

Statistical Programmer- Future Roles (India)

开发工程限定地区(需当地身份)
公司Syneos Health India Private Limited
薪资未公开
工作地点India
地域资格限定地区(需当地身份)
时区要求日间重叠约 6 小时,基本正常作息
用工类型Full Time
发布时间14 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 India 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。

统计程序员-未来职位(印度)
Syneos Health® 是一家领先的全面整合的生物制药解决方案公司,致力于加速客户成功。我们将独特的临床、医学事务和商业洞察转化为成果,以应对现代市场现实。

我们每天因协作而表现得更好,作为一个团队,每个人都在自己擅长的领域做到最好。我们在一系列关键业务服务中汇聚了众多才华横溢的专家,以支持我们的业务。公司内部的每一个职位都对实现我们“缩短实验室到生命之间的距离®”的愿景至关重要。

了解我们的29,000名员工,他们分布在110个国家已经知道的事情。
在这里工作,处处有意义
为什么选择 Syneos Health

  • 我们热衷于通过职业发展和晋升来培养员工;通过支持性强且积极参与的直线管理;技术及治疗领域培训;同行认可和全面奖励计划。
  • 我们致力于打造“真实的自我”文化——你可以真实地做自己。我们的“真实的自我”文化将我们全球的员工团结在一起,我们致力于照顾好我们的员工。
  • 我们不断建设我们所有人都希望工作的公司,也是客户希望合作的公司。为什么?因为当我们将不同的思想、背景、文化和视角汇聚在一起时,我们能够创造一个让每个人都感到归属感的环境。

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格、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任何发现的问题。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 和相关监管指南(如 ICH)。
  • 保持项目文档、测试、验证/质量控制文档和程序的组织良好、完整且最新,确保具备检查准备能力。
  • 在多个项目之间管理日程和时间限制,根据管理层设定的优先级设定目标,并通过重新安排日常工作量来适应时间表或优先级的变化。制定数据集和输出的规范。
查看英文原文

Statistical Programmer- Future Roles (India)Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Every day we perform better because of how we work together, as one team, each the best at what we do. We bring a wide range of talented experts together across a wide range of business-critical services that support our business. Every role within Corporate is vital to furthering our vision of Shortening the Distance from Lab to Life®.
Discover what our 29,000 employees, across 110 countries already know.
WORK HERE MATTERS EVERYWHERE
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 our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
  • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

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.
  • Minimal travel may be required.

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.

We are always excited to connect with great talent. This posting is intended for a [possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available.
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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