Job Description

Job Responsibilities

1. Write the project programming description document based on the project documentation.
2. Develop, validate and maintain SAS programs for data analysis, reporting and data management, including but not limited to the creation of datasets such as SDTM and ADaM, to ensure compliance with clinical data submission standards.
3. For clinical research reports and regulatory filings, complete the production of high-quality forms, lists and charts (TLFs) to ensure compliance with domestic and international regulatory requirements.
4. Write all other documents in the data submission.
5. Review documents from both internal and external sources, communicate with relevant project personnel, and provide program writing support.
6. Support the development of new technologies, SAS macros and applications.
7. Assist senior SAS programmers in completing various types of clinical trial data statistical analysis services.
8. Complete other related work of the department.

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