Sr Statistical Programmer Analyst

Shanghai, China


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The Position

The Senior Statistical Programmer Analyst (SPA 4) has responsibility for statistical programming support for the Pharma Development, gRED or pRED organizations. He/she leads statistical programming activities and provides end to end statistical programming support in planning, specifying, designing, developing and implementing statistical software solutions for the reporting and analysis of clinical trials in accordance with applicable processes.

  • Prepares and distributes SPA deliverables to clinical study team members across the Project.
  • Uses statistical methodologies, advanced analytics and interactive data visualization to explore and to analyze data, and to communicate findings.
  • Leads statistical programming activities of a set of studies or indication including task assignment for SPA team members and contributes to resource planning.
  • Lead exploratory programming activities at the summarized information or integrated analysis across compound studies. Independently determines, develops and provides technical solutions to a wide range of problems approach.
  • Reviews study documentation prior to start of programming for completeness, accuracy and conformance to study / project / global standards, promoting consistency as appropriate.
  • Determines technical objectives and direction for project(s) selecting fit for purpose tools and methods. Specify, review and implement Analysis Datasets adhering to data standards.
  • Develops approaches to meet exploratory analysis selecting fit for purpose visualization and advanced methodologies across compound studies.
  • Able to identify opportunities to provide stakeholders with data interrogation capabilities.
  • Able to identify visualization opportunities, statistical methodologies to provide stakeholders with data interrogation capabilities with support.
  • Contributes to Risk Assessment of reporting objects. Responsible for accuracy and reliability of results by adhering to risk assessment and QC guidelines. Builds and monitors quality in every aspect of job activities.
  • Assess the risk of the exploratory deliverable:  exploratory analysis outputs, tailored visualization. Responsible for accuracy and reliability of results. Builds and monitors quality in every aspect of job activities.
  • Develops delivery timelines in close collaboration with Biometrics team and other relevant Stakeholders. Influences scope control to minimise scope creep. Negotiates alternative timelines based on resourcing / priority constraints.
  • Recommends and specifies global cross-functional technical and process solutions that can drive efficiency. Contributes to the development of cross-functional level standards, tools, guidelines and processes.
  • Recommends and specifies cross-functional technical and process solutions with a focus on methodologies, advanced analytics and visualizations and new types of data.

Who We Are

A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

The next step is yours. To apply today, click on the "Apply online" button.

Genentech is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status. For more information about equal employment opportunity, visit our Genentech Careers page.


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