1. Reads and analyzes protocol, statistical analysis plan, CRF and other trial design documents and discusses with other team members such with as biostatisticians and data managers.
2. Develops and debugs simple to complex SAS program in a timely manner
3. Implements statistical analysis plan, data preparation, and data manipulation into SAS programs and macros
4. Create analysis datasets, statistical tables, figures, and listing for clinical trial data.
5. Create CDISC standard datasets (SDTM and ADaM)
6. Participates in the validation of SAS programs and analysis datasets
7. Maintains documentation for SAS programs and validation results
8. Leads and coordinates the programming work for projects involving SAS programming if necessary
9. Coordinates timelines in orders to fulfill the needs of other departments
歡迎2026年畢業並正在找尋研發替代役的同學申請!
職位選擇:
Direction 1: Physical Design Engineer
Direction 2: ASIC Physical Design Engineer
Direction 3: DFX Engineer
Direction 4: CAD Tools Development Engineer
Direction 5: Design Verification Engineer
What you’ll be doing:
Key Domains:
• Physical and ASIC Design Implementation
• Backend and Layout Optimization
• Design-for-Excellence (DFX: Test, Manufacturability, Debug)
• Development of CAD/EDA Automation Tools
• Functional and Formal Design Verification
What we need to see:
• MS degree from EE/CS or related majors from a prestigious university.
• Good knowledge in digital circuit design.
• Experience in using Verilog HDL.
• Experience in various EDA tools.
• Fluent in English reading and writing.
• Self-motivated, good team player.
Ways to stand out from the crowd:
• Proven ability to work independently as well as in a multi-disciplinary group environment
• Good command of C/C++ or Verilog programming language.
• Familiar with Perl/Python/Tcl/Shell scripting
應徵方式:
請提供以下資料:
• 英文個人履歷
• 學士+碩士成績單 (中英文皆可)
提交申請:
請將上述資料投遞至104,符合資格者將會收到進一步的聯繫通知。
1. Develop and review the case report form (CRF).
2. Develop and review the database specification.
3. Develop and review the database structure on the database builder.
4. Develop and review the data validation specification.
5. Conduct the database validations including the user acceptance testing.
6. Develop and maintain the CRF library.
7. Develop and maintain the edit checks (ECS) library.
8. Develop and conduct the data review process and dummy data generation.
9. Oversee and coordinate clinical data integration activities as a DMPM.
10. Develop and update the templates of related processes.
11. Develop and manage the working process and standard operating procedures (SOPs).
12. Act as a mentor for the Associate Clinical Data Scientist I
13. Complete other tasks or assignments requested by the Supervisor.