A biotech company in California is looking to add a new Statistical Programmer Consultant to its growing team. This role is 100% remote.
Responsibilities:
- Oversee 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
- Work collaboratively with Clinical Operations, Clinical 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, etc.)
- 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
- Assist with the strategy for process improvement
- Identify new tools to increase efficiency and quality
Qualifications:
- 1+ year of Clinical Trial Programming experience in the Biotechnology, Pharmaceutical or Health-related industry
- Master's Degree in Statistics, Computer Science, Mathematics, Engineering or related discipline
- 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 regards to statistical programming processes, management of statistical programmning projects
- Excellent organizational skills and ability to prioritize tasks
