北京 [切换城市] 北京招聘北京在校学生招聘北京大学/大专应届毕业生招聘

高级统计师

强生(中国)投资有限公司

  • 公司规模:10000人以上
  • 公司性质:外资(欧美)
  • 公司行业:医疗设备/器械

职位信息

  • 发布日期:2020-11-24
  • 工作地点:上海
  • 招聘人数:若干人
  • 工作经验:博士
  • 学历要求:招若干人
  • 语言要求:不限
  • 职位类别:大学/大专应届毕业生

职位描述

Position Summary :

The Senior Statistician provides statistical services including analysis, interpretation, design, and reporting or communication of data evidence for research, development, and/or marketed product needs in Janssen. This position supports statistical aspects of business-critical and/or regulatory commitments. He/She abides by the Credo and practices J&J Leadership Imperatives for Individuals: Lead, Shape, Connect, and Deliver.


Key Responsibilities:

1.Expertise: Demonstrates advanced data analytic expertise based on a foundation of statistical principles and a track record of applied experience. Is effective in the use of relevant computational tools for study, experiment, or trial research objectives. Applies high quality statistical methodology in assigned projects with demonstrated understanding of the disease/scientific/functional area and health authority acceptability. Ensures application of appropriate statistical methods and generation of accurate and reproducible results working independently or by providing specifications to statistical programming colleagues. Produces clear, concise, well-organized, and error-free computer programs and statistical reporting content.

2.Quality and Compliance: Complies with organization and company standard operating procedures in timely fashion, such as training and project time accounting. Understands and aligns with relevant regulatory guidances. Contributes high quality and timely deliverables as assessed by stakeholders such as the project team, the clinical trial team, and the Statistics Area Head. Ensures that documents, specifications, programs, and macros are consistent and comply with project and company standards. Follows best practices for Data Integrity.

3.Drug Development: Acquires and demonstrates knowledge in pharmaceutical research and development strategies and execution. Assists in providing experimental design, modeling, analysis planning, analysis execution, interpretation, and statistical communications support. Is accountable for execution of individual project responsibilities, including:meetings with necessary project team members,reporting activities,exploratory analyses/graphics,and additional analyses to support publications for individual clinical trials/studies/projects. Provides critical input to the statistical lead or team in optimizing study or trial designs in line with study or trial objectives and supports scenario simulations and sample size calculations based on relevant technical and disease/scientific/functional area knowledge.

4.Collaboration: Establishes and maintains effective and efficient interfaces and relationships with internal and external customers, with support of Statistics & Decision Sciences (SDS) management. Routinely contributes to area (e.g. discovery, translational, early development, late development) project meetings. Contributes positively to SDS team dynamics with a clear understanding of the SDS vision.

5.Programming: Demonstrates full proficiency in SAS or R, as well as a working knowledge of other relevant computational tools as required.

6.Process: Deep knowledge of data architecture, such as Data Standards. Recognizes the need and value of process standardization.

7.External Engagement: Participates as a member of professional organizations, such as attending meetings sponsored by professional organizations.


Other Responsibilities :

Discovery & Translational 

-Serves as initial consultation contact for new projects. Maintains and grows customer base, and builds loyal relationships with customers.

-Assumes independent, professional responsibility for all phases of a project request from beginning through completion, with minimal supervision as needed.

-Manages multiple projects.

-Documents projects in sufficient detail for reproducibility. 


Manufacturing & Toxicology 

-Serves as initial consultation contact for new projects. Maintains and grows customer base, and builds loyal relationships with customers.

-Assumes independent, professional responsibility for all phases of a project request from beginning through completion, with minimal supervision as needed.

-Manages multiple projects.

-Documents projects in sufficient detail for reproducibility, including entry in project tracking systems and placement into shared repositories. 


Medical Affairs 

-Provides statistical support to Medical Affairs studies and assumes responsibilities for planning, design and analysis of randomized clinical trials, observational studies and/or patient registries for post marketing commitments/requirements and reporting related activities. Applies sound statistical thinking and computational abilities in support of Medical Affairs goals & objectives.

-Contributes in the planning, design, conduct and analysis for clinical trials, observational studies and other types of clinical research projects including but not limited to post-hoc analyses, investigator initiated studies, publications, and HECOR/Epidemiology/Market Access support; Develops statistical analysis plans (SAPs) and data presentation specifications (DPSs); Provides statistical support for all LCM/regulatory-submission related activities; Interacts with other Medical Affairs functional groups (e.g. HECOR/Epidemiology, Market Access and publication teams); in close partnership with statistical lead, interacts with outside investigators (KOLs and vendors) in the preparation of scientific presentations and manuscripts and pursues implementation of robust statistical analyses in support of business-critical evidence generation; Explores and implements innovative statistical methods. 


Requirements:

1.Ph.D. in Statistics or Biostatistics, graduate between Jan. 2020 and Sept. 2021.

2.Basic knowledge of SAS or R programming.

3.Good written, oral, and interpersonal communication skills.


Working location:

Shanghai, Beijing


公司介绍

强生是全球具综合性、业务分布范围广的医疗保健企业,业务涉及消费品、制药、医疗器材三大领域,1985年在华创立了***家合资企业。强生遵循企业信条的价值观,致力于践行“关爱全世界,关注每个人”的健康愿景,以领先的科技研发创造创新的理念、产品和服务,为改善人类健康和福祉而不懈努力。每天,强生遍布世界各地的员工,与他们的合作方一起,为全球消费者和病患带来更健康、更快乐、更长寿的生活。
强生于1985年在华创立了***家合资企业。 多年来,强生不断发挥行业领军作用,以创新、高质量的产品和服务,为中国亿万家庭带来健康。如今,强生在中国的业务涉及消费品、制药、医疗器材三大领域,在北京、上海、广州、苏州、西安等90多个城市,拥有员工总数近10,000人。强生在西安高新技术产业开发区投资兴建先进的大型生产基地,以更好地服务中国和亚太地区其他国家。
强生是***在中国成功实现“端到端”研发模式的跨国企业;并通过实现从早期研发到临床应用,致力于加速中国创新产品的研发,促进中国创新型经济的发展。强生的三大业务领域在中国均设有研发机构, 并在上海建立了强生亚太创新中心,将源自于中国和亚太区域的创新成果推向国际市场。
该创新中心是强生深化外部合作战略的主要窗口。强生将密切与创新企业、学术和科研机构,以及优秀人才的合作,通过提供资金、专业知识和技术,共同将雏形创新转化为医学临床应用的成果,强生并在中国建立全球肺癌研究中心,以满足中国及国际市场的需求,造福病患。
强生心系中国的发展和进步,致力于成为优秀的企业公民。强生积极参与各类重大活动,助力中国的社会经济发展, 并荣幸的成为2008年北京奥运会及残奥会和2010年上海世博会美国馆的全球合作伙伴。
为加强对中国市场的承诺,强生于近期部署了中国发展新战略。强生将融汇全球的资源、凝聚在华的核心业务能力,更加稳健的迈开公司积极创新、完美执行和锐意领先的步伐,为中国创造更多价值。
强生多次荣获《巴伦周刊》“全球最受尊敬企业”的荣誉,充分体现了强生始终以实际行动改善人类健康福祉的不变理念。
2017年,强生连续第33年入选美国《财富》杂志发布的全球最受赞赏企业排行榜,位列总榜第13名,居全球制药行业榜首。

联系方式

  • Email:cke1@its.jnj.com
  • 公司地址:深圳