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Lilly Consultant Computation in 上海, China

Job Category:


Type of Employment:



Primary Function/Purpose

The consultant computation assists during the development of data analysis plans in collaboration with statistical colleagues, physicians, and/or medical colleagues. The Statistician-Computation is responsible for establishing a reporting database and for analyzing clinical trial data by working with clinical research associates/clinical development associates and project statisticians.

Key Responsibilities

The job tasks listed below outline the scope of the position. The application of these tasks may vary, based upon current business needs.

Statistical Trial Analysis

  • Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans.

  • Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the data analysis plan, and conducting the actual analysis once a reporting database is created.

  • Collaborate with data management in the planning and implementation of data quality assurance plans.

  • Maintain proficiency with respect to SAS programming and statistical methodology and in applying new and varied methods.

  • Effectively justify methods selected and implement previously outlined analysis plans.

  • Conduct peer-review of work products from statistical colleagues.

  • Effectively utilize current technologies and available tools for conducting the clinical trial analysis.

Communication of Results and Inferences

  • Collaborate with other statistical colleagues to write reports and communicate results.

  • Responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers.

  • Assist or respond to regulatory queries working in collaboration with other statistical colleagues.

Therapeutic Area and Systems Knowledge

  • Understand relevant disease states in order to enhance the level of customer focus and collaboration.

  • Ensure replication of tools and systems, where applicable and stay informed of technology advances.

Regulatory Compliance

  • Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable corporate, medical, local, and departmental policies, procedures, processes and training.

Basic Qualificiations:


  • B.S, M.S, PhD, or equivalent experience

  • Statistics, Biostatistics, Computer Science, Epidemiology, or equivalent of field study

  • At least 6 years clinical trial working experience

  • CDISC standard hands-on working experience, including writing specifications and programming of SDTM, ADaM, and TFL

  • Proficiency in the SAS programming language

Additional Preferences

  • Capability of working independently

  • Interpersonal/teamwork skills for effectiveness interactions

  • Technical growth and application with working knowledge of statistics and statistical software

  • Self-management skills with a focus on results for timely and accurate completion of completing deliverables

  • Creativity and innovation

  • Demonstrated problem solving ability and attention to details

  • Data analysis, technology, and system expertise

Additional Skills/Preferences:

Additional Information:

Company Overview:

Posted Date:


Region: 亚洲/太平洋地区

City: 上海

State: 上海市

Country: CHN

Location Details:

Req Id: 51686BR