Associate Director, Statistical Programming
Tasks
- Build validate CDISC ADaM specifications and datasets
- Build validate CDISC SDTM specifications and datasets
- Create validate analysis datasets for submissions
- Develop validate global SAS macros
- Develop validate run SAS programs for clinical trial data
- Implement statistical analysis using Biostatistics
- Lead statistical programming delivery for clinical trials
- Manage quality and timely delivery of statistical programming deliverables
- Partner with oversee CROs and programming vendors
- Review provide input to DMP eCRF specifications and SAP
- Write SAS and R code for TLFs tables listings figures
- Write technical programming specifications and reviewer guides
Perks/Benefits
- 401k match
- Dental insurance
- Disability insurance
- Flexible spending account
- Health and well-being benefits
- Health savings account
- Holidays
- Life insurance
- Lifestyle Reimbursement Program
- Medical insurance
- Paid time off
- Vision insurance
- Wellness days
Skills/Tech-stack
Analysis Plan | CDISC ADaM | CDISC SDTM | Clinical data | Clinical data management | Clinical trials | Data Management | Define-XML | R | RStudio Server | S&OP | SAS | SAS Base | SAS Graph | SAS Macro | SAS SQL | SAS Stat | Statistical Analysis | Statistical Analysis Plan | TLF
Education
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