What are the responsibilities and job description for the Statistical Programmer II position at Katalyst Healthcares & Life Sciences?
Responsibilities:
- Involve in the programming activities on multiple projects/ studies across various therapeutic areas, both internally and externally by CROs.
- Create and review annotated CRF to SDTM datasets.
- Provide support in balancing conflicting priorities, promoting communication and adequate information flow to motivate,encourage and align people with the company's strategic objectives.
- Function as a positive role model for setting high expectations for quality, creativity and project ownership.
- Works collaboratively with Clinical Operation, Data Management,Global Drug Safety, Regulatory and Project Management management/staff to meet project deliverables and timelines for statistical data analysis and reporting.
- Provide technical input into documents produced by other functions (e.g. biostatisticians, data managers, medical writers.
- Work with Biometrics and other functions for the development and maintenance of the data review and reporting tools, and any other statistical applications as appropriate.
- Involved with the strategy for process improvement.
- Identify new tools to increase efficiency and quality.
- Master's Degree in Statistics, Computer Science, Mathematics, Engineering or related discipline.
- Minimum of 1-5 years of clinical trial programming experience in the biotechnology, pharmaceutical or health related industry.
- Advanced SAS programming skills and experience in other statistical software, such as R and S-Plus.
- Experience and in-depth knowledge in CDISC including SDTM, ADaM, and controlled terminologies.
- Self-directed, technically strong, and a recognized leader maintaining a strategic prospective with regard to statistical programming processes, management of statistical programing projects.
- Excellent organizational skills and ability to prioritize tasks.
