Key skills
Statistical Analysis
About this role
Role Overview
- Support coordination, delivery, and review of statistical programming outputs across assigned studies
- Develop CDISC ADaM analysis datasets and specifications; identify and flag data quality issues
- Contribute to end-to-end programming from CRF data collection through regulatory submission
- Support preparation of submission deliverables (define.xml, XPTs, reviewer documentation)
- Collaborate with Biostatistics, Data Management, and Data Standards to ensure consistency and compliance
- Assist with process improvement initiatives and departmental efficiency efforts
Requirements
- Bachelor’s degree in Statistics, Mathematics, or related field
- 0–2 years of SAS programming experience (Base, STAT, GRAPH, MACRO)
- Exposure to clinical trials, data management, or statistical analysis
- Basic knowledge of CDISC standards and clinical data structures
- Understanding of drug development process and regulatory requirements
Benefits
- Medical, Dental, Vision, & Life insurances
- Fitness & Wellness programs including a fitness reimbursement
- Short
- and Long-Term Disability insurance
- A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
- Up to 12 company paid holidays + 3 paid days off for Personal Significance
- 80 hours of sick time per calendar year
- Paid Maternity and Parental Leave benefit
- 401(k) program participation with company matched contributions
- Employee stock purchase plan
- Tuition reimbursement of up to $10,000 per calendar year
- Employee Resource Groups participation