Lead Statistical Programmer – Oncology Trials

Revolution Medicines; San Francisco (CA); On-site; USD 164,000 - 205,000; Full time

Job summary

Revolution Medicines is seeking a Senior Statistical Programmer with 10–14 years of experience in oncology trials to lead programming activities across early to late‑phase programs. You will oversee internal and CRO resources, ensure CDISC‑driven deliverables, and support regulatory submissions while mentoring teammates in RevMed values and scientific rigor.

The role emphasizes quality, timely delivery, and collaboration across interdisciplinary teams to advance innovative oncology therapies.

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.

Responsibilities

• Provide technical oversight of statistical programming resources including contractors and CROs.
• Provide mentorship to future leaders to help learn and execute on RevMed core values.
• Ensure quality and timely delivery of analysis for statistical programming deliverables.
• Provide solutions by analyzing issues and problems in complex situations.
• Ensure accuracy of clinical trial results for internal and external audiences via QC of documents with clinical data.
• Ensure that the statistical programming process conforms to SOPs and regulatory standards where applicable.
• Timeline and vendor management for deliverables, including submission‑related activities, complying with regulatory standards.
• Programming support for deliverables such as Dose Committee meetings, Investigator Brochures, publications/presentations, US and ex‑US regulatory submissions.
• Proficiency in regulatory standards and compliance regulations including CDISC (SDTM, ADaM, define.xml, Reviewer’s Guides).

Skills

Statistical programming

Leadership

Regulatory compliance

Education

BS/BA degree

Tools

CDISC (SDTM/ADaM)

Job description

Revolution Medicines is seeking a Senior Statistical Programmer with 10–14 years of experience in oncology trials to lead programming activities across early to late‑phase programs. You will oversee internal and CRO resources, ensure CDISC‑driven deliverables, and support regulatory submissions while mentoring teammates in RevMed values and scientific rigor.

The role emphasizes quality, timely delivery, and collaboration across interdisciplinary teams to advance innovative oncology therapies.