Lead Statistical Programmer – Oncology Trials

Revolution Medicines; San Francisco (CA); On-site; USD 150,000 - 190,000; Full time

Job summary

Revolution Medicines, Inc. 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 and drive CDISC‑driven deliverables. You will support regulatory submissions, ensure high-quality timelines, and mentor teammates while upholding RevMed values and scientific rigor in a collaborative, cross-disciplinary environment.

Qualifications

• 10–14 years of experience in statistical programming for oncology trials.
• Strong SAS programming and SAS Macro skills.
• CDISC SDTM/ADaM deliverables experience.
• Experience with regulatory submissions (e.g., IND/CTD, submission deliverables).
• Mentor and lead programming teams across projects.

Responsibilities

• Lead programming activities across early to late‑phase oncology programs.
• Oversee internal and CRO resources.
• Drive CDISC‑driven deliverables for trials and submissions.
• Support regulatory submissions with high-quality programming outputs.
• Mentor teammates and promote scientific rigor and collaboration.

Skills

SAS

CDISC standards

Clinical trials

Oncology

Leadership

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.