Associate Principal Statistical Analyst
$164,000–$205,000 year
HybridRedwood City, California, United States
Job Summary
Provide technical oversight of statistical programming resources, including contractors and CROs, while ensuring quality and timely delivery of analysis for statistical programming deliverables. Mentor future leaders to execute on core values and solve complex issues by analyzing problems in clinical trials. Ensure accuracy of clinical trial results for internal and external audiences via QC of documents with clinical data, maintaining conformance to SOPs and regulatory standards such as CDISC and FDA 21 CFR Part 11. Manage timelines and vendor deliverables for regulatory submissions, including Dose Committee meetings, Investigator Brochures, and publications. Requires 10-14 years of statistical programming experience in oncology clinical 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
Desired Qualifications
- Early or late-stage oncology clinical trials
- A demonstrable record of strong leadership and teamwork
- Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high energy environment
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