出海雷达

Statistical Programmer III / Senior Statistical Programmer

开发工程限定地区(需当地身份)
公司Aixial Group
薪资未公开
工作地点Romania
地域资格限定地区(需当地身份)
时区要求日间重叠约 3 小时,需偶尔早起或晚睡
用工类型Full Time
发布时间今天
数据来源Himalayas
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注意地域限制:该职位明确限定在 Romania 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。
关于本页中文:职位描述由本机离线模型翻译,属机器翻译,供快速判断用;正式沟通与投递请以英文原文为准。官方翻译通道恢复后会自动重译升级。

我们是谁?收获综合研究组织 (HiRO) 是一个全球性导向,创新性的临床研究组织 (CRO).通过全球运营和集成能力,HiRO 为客户提供了全系列跨境解决方案和服务,包括早期临床前战略规划,临床试验设计,监管事务,药物警,统计,数据管理,端到端项目管理以及临床和医疗监测服务。作为一个新兴的全球 CRO,HiRO 致力于成为市场领先的综合全球临床研究组织,与生物技术和制药公司合作将新的产品从实验室推出到市场,为世界各地患者提供更有效的解决方案。THE ROLE 目前我们正在寻找两个热情和有才华的统计程序员 III,愿意参与所有活动范围,包括担任研究领导者。这个角色与内部部门以及外部各方兼职。该角色在罗马尼亚本地工作。关键责任 · SDTM 数据集的研究规范和 QC 创建,以及 SDTM 数据集 I-IV 阶段试验的统计编程和 QC. · ADaM 数据集的学习规范和 QA 创建,I-IV 阶级试验的 ADaM 数据组的统计计划和 QC; · I-IV 期试验表表,列表和数字的统计程序和 QC·负责分配的统计成果质量和及时性。· 作为首席统计程序员,主要负责所有分配研究上的统计编制活动,包括分配的统計编程团队成员的活动的规划和协调。·积极参与部门流程和程序的改进。(高级统计编程师)·在统计编制团队内提供导师。(高级数据编程师).资格和属性 ·计算机科学,数学,统计学,生命科学或相关领域等级;•至少有4-5年的经验工作 CRO·最低5-6年的经验为 CRO (高级统計编程师); •优秀的 SAS 编程技能 (BASE,MACRO,GRAPH). ·对 CDISC 标准的卓越知识。·具有统计编辑计划创业和过程开发的经验。·

查看英文原文

Who we are?
Harvest Integrated Research Organization (HiRO) is a globally oriented, innovative clinical research organization (CRO). With global operations and integrated capabilities, HiRO provides a full range of cross-border solutions and services to its clients, including early pre-clinical strategic planning, clinical trial design, regulatory affairs, pharmacovigilance, statistics, data management, end-to-end project management, and clinical and medical monitoring services. As an emerging global CRO, HiRO strives to become a market-leading, integrated global clinical research organization that works collaboratively with biotech and pharmaceutical companies to bring new products from the laboratory to the market, providing more effective solutions for patients worldwide.
THE ROLE
We are currently looking for two enthusiastic and talented Statistical Programmers III, willing to be involved in all spectrums of activities, including acting as Lead on studies. This role works cross-functionally with internal departments and with external parties as well.
This role is home-based in Romania.
Key responsibilities

  • Creation and QC of study specifications for SDTM datasets, and statistical programming and QC of SDTM datasets for Phase I-IV trials.
  • Creation and QC of study specifications for ADaM datasets, and statistical programming and QC of ADaM datasets for Phase I-IV trials.
  • Statistical programming and QC of tables, listings and figures for Phase I-IV trials.
  • Responsible for the quality and timeliness of assigned statistical deliverables.
  • As Lead Statistical Programmer, primarily responsible for all statistical programming activities on assigned studies including planning and coordination of activities for assigned statistical programming team members.
  • Active participation in improvements to departmental processes and procedures. (Senior Statistical Programmer)
  • Provide mentoring within the Statistical Programming team. (Senior Statistical Programmer)

Qualifications and attributes

  • BSc/BA or equivalent in computer science, mathematics, statistics, life sciences or related field(s).
  • Minimum of 4-5 years of experience working for a CRO
  • Minimum of 5-6 years of experience working for a CRO (Senior Statistical Programmer)
  • Excellent SAS programming skills (BASE, MACRO, GRAPH).
  • Excellent knowledge of CDISC standards.
  • Experience in statistical programming initiatives, and development of processes.
  • Knowledge and experience in database design and structures.
  • The ability to perform all duties as a statistical programming project team member with no supervision.
  • The ability to perform all duties of Lead Statistical Programmer on several concurrent studies without supervision.
  • Very good knowledge of clinical trial practices, procedures, and methodologies.
  • Expert knowledge of clinical trial practices, procedures, and methodologies. (Senior Statistical Programmer)
  • Strong oral and written communication skills.
  • Excellent organizational/time management skills.
  • An excellent investigative and meticulous approach to all activities and tasks

What we offer:

  • Mentorship and training to develop your skills in the clinical trials industry.
  • The chance to be part of an effective, dynamic, friendly, and supportive team.
  • Work with new and exciting technologies.
  • Development opportunities.

For more information about HiRO Company, please visit our page:
We also encourage you to follow our company page on Linkedin for the most up to date company news and job postings.
Originally posted on Himalayas

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