Assoc Director, Statistical Programming

Associate Director, Statistical Programming (Hybrid; Foster City, CA or Raleigh, NC; NOT fully remote)

Job Responsibilities:
- Collaborate with Clinical Development to meet statistical analysis/reporting deliverables and timelines.
- Generate/oversee programming deliverables (tables, listings) for study reports and integrated summaries.
- Anticipate resource needs; ensure programming and documentation follow departmental procedures.
- Direct design/coding of analysis files; provide primary/secondary programming support and harmonize process-improvement initiatives.
- Apply strong communication skills; define and produce user-defined/ad hoc statistical reports with other departments.
- Anticipate and resolve study issues/conflicts; act as a key resource on multiple time-sensitive complex tasks.
- Create buy-in, negotiate timelines, manage critical deadlines, and lead programming-group strategic initiatives.

Basic Qualifications:
- BS (Biostatistics/Computer Science or equivalent) + 10+ years pharma/biotech experience
- OR MS + 8+ years
- OR PhD + 3+ years

Preferred Qualifications:
- 10+ years pharma/CRO experience; oncology/hematology/virology/inflammation experience; submission knowledge
- Pivotal studies + integrated analysis + regulatory submission activities
- SAS (including macros); CDISC (CDASH, SDTM, ADaM); GCP/ICH; complex fast-turnaround experience

Compensation/Benefits (if applicable): Bay Area $195,670–$253,220; Raleigh $168,980–$218,680. May include annual bonus, stock incentives, paid time off, and medical/dental/vision/life insurance.

Application Instructions (for current employees/contractors): Apply via the Internal Career Opportunities portal in Workday.