Clinical Systems Associate
Revolution Medicines · Redwood City, California, United States
Posted 12 days ago
or apply directly on Revolution Medicines's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 12 days Revolution Medicines's roles stay open a median of 43 days
- Reposted
- No
- Salary listed
- No 0% of Revolution Medicines's roles list one
- Ghost-job risk at Revolution Medicines
- low 0 stale, 6 reposted of 264 open
- Hiring momentum
- 449 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Revolution Medicines's own greenhouse board since 2026-08-03. Full hiring picture for Revolution Medicines.
About this role
The Clinical Systems Associate at Revolution Medicines will be responsible for developing and maintaining dashboards and reports to support clinical trial data review and operational insights. The role involves programming and automation using SAS and R, software validation, system management, and providing training and user support. Collaboration with cross-functional teams is essential to enhance data quality and project coordination.
- benefits
- 1/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 4/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Revolution Medicines as an employer.
What you need
- Bachelor’s degree in Computer Science, Health Informatics, Biostatistics, or a related field (or equivalent experience in clinical data and programming)
- 4 years of experience with SAS, SQL, and R programming for clinical data analysis, including dataset manipulation and TFL generation and verification
- Experience with dashboard development and web page design
- Familiarity with clinical trial data standards (e.g., SDTM, ADaM) and data cleaning processes
- Understanding software validation processes (IQ, OQ, PQ, UAT) and GxP compliance
- Strong attention to detail, data integrity, and traceability in a regulated environment
Nice to have
- Direct experience with clinical trial data in a pharmaceutical or biotech setting
- Experience supporting the development and validation of ADaM datasets and TFLs for regulatory submissions
- Familiarity with clinical data visualization and reporting tools (e.g., R Shiny, Power BI)
- Exposure to clinical systems such as CTMS, EDC, or statistical computing environments
- Experience delivering training and documentation to support user adoption of clinical systems and tools
Worth weighing
- Base pay salary range is $120,000 — $150,000 USD, but may vary based on location and other factors
- No specific benefits listed in the posting
- Role involves working in a regulated environment, which may require strict adherence to compliance standards
Summarised from Revolution Medicines's posting. Read the full original.
Listed by Revolution Medicines on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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