Associate Director, Statistical Programming
Tasks
- Collaborate with biostatistics clinical data management pharmacovigilance and clinical operations
- Conduct programming plans resource allocation and prioritization
- Develop and validate SAS programs for analysis datasets
- Develop and validate analysis dataset specifications
- Ensure SOP compliance
- Generate analysis tables listings figures and graphs
- Lead and manage statistical programmers
- Maintain programming infrastructure
- Oversee statistical programming for clinical studies
- Review and update programming processes
- Support clinical and statistical programming team management
- Support electronic submission file creation eCTD
Perks/Benefits
- Dental insurance
- Equity awards
- Health insurance
- Incentive bonus
- Paid time off
- Retirement plan
- Vision insurance
Skills/Tech-stack
21 CFR | 21 CFR Part 11 | Alexion standards | CDISC ADaM | CDISC SDTM | CFR Part 11 | Clinical Practice | ECTD | Good Clinical Practice | Good Programming Practice | Inform | Integrated Summary | Integrated Summary Safety Efficacy | Medidata | Oracle | Part 11 | Relational databases | SAS | SAS Base | SAS Graph | SAS Macro | SAS SQL | SAS Stat
Education
Bachelor of Engineering | Bachelor of Science | Master of Arts | Master of Science
Regions
Countries
States
Cities
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