面議（經常性薪資達4萬元或以上） 台北市內湖區 3年工作經驗 今天剛更新
The Senior Programmer I works independently on medium to large size/complexity clinical trial projects. The person will be either extremely strong technically and/or have strong team leadership skills and good technical knowledge. The essential functions are:
1. Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs
2. Leads statistical programming activities across multiple studies
3. Produce, and co-ordinate the production of, all tables, listings, and figures for medium to high complexity clinical trial programs including ISS, ISE, Canada using SAS
4. Either extremely strong SAS skills (with ability to debug, troubleshoot, and review medium complexity SAS programs including use of macros, SAS graph, PROC SQL) or strong SAS skills (with ability to debug, troubleshoot, and review medium complexity SAS programs including use of macros, SAS graph, PROC SQL) combined with strong leadership/coordination skills
5. Lead the SAS programming for a clinical trial program for one or more of LLX SOLUTIONS, LLC‘s major clients
6. Working knowledge of R programming for statistical analysis, visualization, and exploratory data review
7. Provide leadership, SAS code quality review, and mentoring to less experienced programmers, which may include coordinating the work of a team of programmers
8. Ensure all work, including work of team where responsible, is processed on time to appropriate quality levels and within budget
Additional Responsibilities:
1. Represent LLX SOLUTIONS, LLC at client marketing and technical meetings
2. Review and provide programming input to protocol, CRF, data handling document, validation checks
3. Estimate resources and timelines in the proposal process
4. Participate in and/or lead process/quality improvement initiatives
5. Help with recruitment of programmers
6. Achieve or exceed personal billability targets
Additional tasks already included in responsibilities of lower level positions:
1. Very good understanding of the tasks and assumptions for the project contract and the time allowed for the programming functions to be performed.
2. Very good understanding of clinical trial documentation to acquire a basic knowledge of the therapeutic area and understand the objectives of the protocol.
3. Work to the specifications in an analysis plan, related SOPs, and guidelines.
4. Keep informed of programming techniques as applied to clinical trials by reading relevant journals and attending courses I programming meetings.
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