Associate Principal Statistical Analyst
$164,000–$205,000 year
Hybrid · Redwood City, California, United States
Job Summary
Associate Principal Statistical Analyst responsible for providing technical oversight of statistical programming resources (including contractors and CROs), mentoring future leaders, and ensuring high-quality, timely delivery of analyses for oncology clinical trials. Role involves regulatory-submission support with adherence to CDISC standards (SDTM, ADaM, define.xml, Reviewer’s Guides), SOPs, and GxP; timeline and vendor management for deliverables (e.g., Dose Committee meetings, Investigator Brochures, publications/presentations, US and ex-US regulatory submissions); proficiency in regulatory standards and compliance; and collaborating in an interdisciplinary team to drive innovative approaches in a high-energy environment. Base pay is disclosed for onsite Redwood City, CA, with #LI-Hybrid indicating a hybrid work arrangement. Preferred candidates will have leadership experience, strong teamwork, and a track record in early- or late-stage oncology trials.
Required Qualifications
- 10-14 years of Statistical Programming experience in biotechnology or pharmaceutical industry
- BS/BA degree or other suitable qualification with relevance to the field
- Direct statistical programming experience for early or late-phase clinical trials to support production/verification of analysis datasets, tables, listings, and figures
- Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute goals as a member of an interdisciplinary team
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.