Clinical Systems Associate

Socket.dev; Redwood City (CA); On-site; USD 120,000 - 150,000; Full time

Job summary

Revolution Medicines in Redwood City, CA seeks a skilled clinical data professional to build and maintain dashboards and reports supporting clinical trial data review, performance metrics, and operational insights across Biostatistics, Clinical Data Science, Clinical Systems, Medical Science, and Statistical Programming.

Responsibilities include developing SAS, SQL, and R scripts for data cleaning and reporting; validating GxP systems (IQ/OQ/PQ/UAT); maintaining system documentation; and

Qualifications

• Bachelor’s degree in Computer Science, Health Informatics, Biostatistics, or a related field (or equivalent experience).
• 4 years of experience with SAS, SQL, and R programming for clinical data analysis including dataset manipulation and TFL generation/verification.
• Experience with dashboard development and web page design.
• Familiarity with SDTM/ADaM data standards and data cleaning processes.
• Understanding of IQ/OQ/PQ/UAT software validation and GxP compliance.
• Strong attention to detail, data integrity, and traceability in a regulated environment.
• Ability to manage multiple projects and communicate technical concepts across diverse teams.

Responsibilities

• Develop and maintain dashboards and reports supporting clinical trial data review and operational insights.
• Create SAS/R/SQL scripts for data cleaning, transformation, and reporting.
• Validate clinical systems (IQ/OQ/PQ/UAT) and maintain related documentation.
• Support controlled clinical analysis systems, ensuring availability, performance, and compliance.
• Prepare onboarding materials and provide training for clinical systems and data tools.
• Collaborate cross-functionally with Biostatistics, Clinical Data Science, Clinical Operations and IT to accelerate data cleaning and improve data quality.

Skills

SAS/SQL/R programming

Dashboard development

Data visualization

Communication

Education

Bachelor’s degree in Computer Science or Health Informatics or Biostatistics

Tools

SAS

SQL

R

HTML

CSS

Power BI

Job description

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.

Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.

The Opportunity:

• Dashboard and Data Review Support: Developing and maintaining dashboards and reports that support clinical trial data review, performance metrics, and operational insights across Biostatistics, Clinical Data Science, Clinical Systems, Medical Science, and Statistical Programming.
• Programming and Automation: Develop and maintain scripts using SAS and R to support data cleaning, transformation, and reporting. Create utility tools to automate repetitive tasks and improve data processing efficiency.
• Software Validation: evaluate and implement GxP-compliant clinical systems (including programming environment and data platforms). Collect requirements, interpret specifications, and work with IT to prepare IQ, OQ, PQ, and UAT test cases.
• System Management and Maintenance: Support controlled clinical analysis systems, ensuring system availability, performance, and compliance. Maintain documentation for folder access control, system patches, and change management.
• Training and User Support: Prepare and deliver onboarding materials and training sessions for clinical systems and data tools. Enhance user engagement by providing clear, accessible documentation and ongoing support.
• Cross-Functional Collaboration: Work closely with Biostatistics, Clinical Data Science, Clinical Operations, and IT to understand data review needs, provide solutions to accelerate data cleaning, and improve data quality across clinical systems.
• Project Coordination: Assist in tracking project timelines, deliverables, and dependencies. Support meeting organization, documentation, and follow-up across multiple priorities.

Required Skills, Experience and Education:

• 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.
• Ability to manage multiple projects and communicate technical concepts across diverse teams.

Preferred Skills:

• 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.
• Experience with HTML and CSS for web page development.
• Experience with version control systems (e.g., Git) for managing scripts and documentation.

#LI-DN1 #LI-Hybrid

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Base Pay Salary Range

$120,000 — $150,000 USD

Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.

Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact [e-mail].