Role Summary
The Director of Statistical Programming will focus on applying programming methodology for implementing statistical analyses using SAS for in-house deliverables and performing quality review of outsourced statistical deliverables. They will participate as active members of a cross-functional team to plan, lead and execute the tasks required to support the assigned programs.
Responsibilities
- Provide statistical programming leadership for an assigned indication that may consist of multiple clinical trials
- Work closely with biostatisticians to review the SAP, and responsible in the development of data/analysis program specification based on the SAP
- Maintain complete and auditable programming documentations for analysis of clinical trials
- Contribute to the development, documentation and maintenance of reusable programming code library
- Collaborate with IT to set-up/maintain the statistical computing infrastructure (e.g., SAS server)
- May act as a biostatistician on small-scale projects
- Collaborate with various functions to ensure robust CRF/EDC development, and quality data collection for the assigned clinical trials
- Oversee the biometrics vendors to ensure the prompt and quality statistical deliverables
- Provide quality review of outsourced statistical deliverables (including inhouse double programming to QC as needed) and coordinate the inhouse review comments
- Contribute to the development of functional-level standards, SOPs, and work instructions and templates
- Stay abreast of industry development in biostatistics/statistical programming fields and apply to appropriate systems and processes
- Other duties as assigned, nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time
Qualifications
- Required: B.A./B.S. degree in statistics, computer science, or other quantitative science
- Preferred: Advanced degree (M.A./M.S.) or equivalent experience
- Required/Preferred: B.A./B.S. with 17+ years, or M.A./M.S. with 13+ years
- Preferred: Experience in ophthalmology and/or biologic/gene therapy
Skills
- Strong SAS programming skills required with proficiency in SAS/BASE, SAS Macros, SAS/Stat and ODS (proficiency in SAS/SQL, SAS/GRAPH or SAS/ACCESS is a plus)
- Proficiency in R programming a plus
- Proficiency in Microsoft Office Apps, such as WORD, EXCEL, and PowerPoint (familiar with the “Chart” features in EXCEL/PowerPoint a plus)
- Good understanding of standards specific to clinical trials such as CDISC, SDTM, and ADaM, MedDRA, WHODRUG
- Experience with all clinical phases (I, II, III, and IV) is desirable
- Experience with BLA/IND submissions is strongly desirable
- Good understanding of regulatory requirements for submission-related activities (e.g., CDISC, CDASH, eCTD) and CRT packages (e.g., XPTs Define/xml, reviewer’s guide, analysis metadata report, executable programs) is desirable
- Able to run the P21 checks is a plus
- Knowledge of applicable GCP/FDACHMP//ICH/HIPAA regulations
- Displays excellent organization and time management skills, excellent attention to detail, and ability to multi-task in a fast-paced environment with shifting priorities and/or conflicting deadlines
- Excellent written and verbal communication skills and strong team player with a demonstrated track record of success in cross-functional team environment
- Proven conceptual, analytical and strategic thinking
- Good interpersonal and project management skills
- Proactively identifies risks, issues, and possible solutions
Education
- Bachelor's degree in statistics, computer science, or another quantitative science field required
- Master's degree (M.A./M.S.) preferred, or equivalent experience
Additional Requirements
- Travel: <5%
- Physical Activity: Repetitive motions involving wrists, hands, and fingers; typing or manipulating small objects
- Physical Requirements: Sedentary work requiring occasional lifting up to 10 pounds
- Working Conditions: Not substantially exposed to adverse environmental conditions