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Clinical R Programmer Jobs in Mountain View, CA (NOW HIRING)

CYNET SYSTEMS

Clinical Data Manager

Sunnyvale, CA · On-site

$70 - $75/hr

Support clinical data review requirements from Lead data manager. * Create customise data review ... Excellent hands on experience on SAS or R programming language for data review listings/tracker.

Recor Medical

Senior Clinical Programmer

Palo Alto, CA

$145.60K - $156.35K/yr

Proficiency in R, with experience in other relevant programming languages (e.g., Python, SQL, SAS). * Comprehensive understanding of clinical trial processes, data flow, and clinical trial data ...

Jj

Clinical Engineer

Santa Clara, CA · On-site

Santa Clara, California, United States of America Clinical Engineer Robotics and Digital Solutions, part of Johnson & Johnson MedTech family of companies, is recruiting for a Clinical Engineer for ...

Johnson & Johnson

Clinical Engineer

Santa Clara, CA · On-site

Santa Clara, California, United States of America Clinical Engineer Robotics and Digital Solutions, part of Johnson & Johnson MedTech family of companies, is recruiting for a Clinical Engineer for ...

Exelixis

Statistical Programming Manager

Alameda, CA · On-site

... • If the lead programmer on studies, works with clinical data management staff and ... R, Tableau, CDISC, and SAS/GRAPH experience desirable. • Ability to communicate verbally and in ...

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How much do clinical r programmer jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for clinical r programmer in Mountain View, CA is $76.41, according to ZipRecruiter salary data. Most workers in this role earn between $63.22 and $86.49 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical R Programmer, and why are they important?

To thrive as a Clinical R Programmer, you need a solid background in statistics, R programming, and clinical trial data analysis, often supported by a degree in statistics, biostatistics, or a related field. Expertise in SAS, CDISC standards (SDTM/ADaM), and familiarity with clinical data management systems are commonly required. Attention to detail, problem-solving skills, and effective communication enable you to interpret data accurately and collaborate with cross-functional teams. These skills are vital for ensuring reliable statistical outputs that support regulatory submissions and data-driven decisions in clinical research.

What are some common challenges faced by Clinical R Programmers when working with clinical trial data?

Clinical R Programmers often encounter challenges such as handling large and complex datasets, ensuring strict compliance with regulatory standards (like CDISC SDTM and ADaM), and maintaining data integrity throughout the analysis process. Collaboration can be demanding, as programmers must frequently coordinate with biostatisticians, data managers, and clinical teams to interpret data requirements and resolve discrepancies. Staying updated with evolving industry guidelines and managing tight project timelines are also common aspects of the role.

What are Clinical R Programmers?

Clinical R Programmers are professionals who use the R programming language to manage, analyze, and visualize clinical trial data in the pharmaceutical, biotech, or healthcare industries. They play a key role in preparing statistical reports, generating tables, listings, and figures (TLFs), and ensuring data integrity for regulatory submissions. Clinical R Programmers collaborate with statisticians, data managers, and clinical teams to ensure the accuracy and compliance of clinical trial results with industry standards and regulatory requirements.

What is the difference between Clinical R Programmer vs Clinical SAS Programmer?

AspectClinical R ProgrammerClinical SAS Programmer
Required CredentialsTypically requires a degree in statistics, biostatistics, or related field; proficiency in R programmingUsually requires a degree in statistics, biostatistics, or related field; proficiency in SAS programming
Work EnvironmentOften works in research-focused settings, academia, or biotech companies using open-source toolsCommonly employed in pharmaceutical companies, CROs, and clinical trial data analysis using SAS
Industry UsageGrowing in popularity for data analysis and visualization in clinical researchStandard in clinical trial data management and regulatory submissions

While both roles involve programming for clinical data analysis, Clinical R Programmers focus on using R for statistical analysis and visualization, whereas Clinical SAS Programmers primarily use SAS for data management and reporting. The choice depends on the company's preferred tools and project requirements.

What are popular job titles related to Clinical R Programmer jobs in Mountain View, CA? For Clinical R Programmer jobs in Mountain View, CA, the most frequently searched job titles are:
What job categories do people searching Clinical R Programmer jobs in Mountain View, CA look for? The top searched job categories for Clinical R Programmer jobs in Mountain View, CA are:
What cities near Mountain View, CA are hiring for Clinical R Programmer jobs? Cities near Mountain View, CA with the most Clinical R Programmer job openings:
Clinical R Programmer jobs near you
Associate Director, Clinical Data Analytics and Reporting

Associate Director, Clinical Data Analytics and Reporting

Eikon Therapeutics

Millbrae, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago

Job description

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.
Position:
The Associate Director, Clinical Data Analytics and Reporting is a leader responsible for establishing and scaling a Clinical Research & Development clinical analytics function for a growing biotechnology company. This role will define the analytics strategy, operating model, and technology roadmap, including the technical implementation to enable high-quality, data-driven decision-making across Clinical Research & Development, with primary focus on oncology programs. This is a hands-on role requiring demonstrated expertise in design, development, test and support of complete analytics & reporting system lifecycle. This leader will partner closely with Clinical Operations, Biostatistics, Data Management, Clinical Research, Regulatory, Safety and Clinical Quality Assurance to ensure proactive risk identification, operational excellence, inspection-ready execution across the portfolio.
About You
The successful candidate will combine deep clinical development expertise with advanced analytics, data governance, and visualization capabilities. The ideal candidate for this role should possess a proven track record of designing, implementing and supporting end-to-end data analytics solutions using current state-of-the-art technologies, and a deep knowledge of emerging trends and best practices in data analytics.
What will you do:
  • Collaborate with Stakeholders in different areas of Clinical Development R&D organization, IT System Owners and external vendors to define and implement the clinical analytics vision, strategy and capabilities (e.g., dashboard, etc.) aligned with clinical development objectives.
  • Establish a scalable analytics operating model suitable for early stage through late phase development.
  • Translate complex clinical and operational data into clear, actionable insights for executive and study teams (including predictive and prescriptive analytics to anticipate risks and optimize trial execution).
  • Design, development, test and deployment of the complete end-to-end analytics solution to enable decision-grade dashboards and metrics across Clinical R&D.
  • Design and implementation of datawarehouse/datalake/lakehouse including star schemas.
  • Collaborate with System Owners, Business Owners and Subject Matter Experts to map sources system objects and attributes to data warehouse objects.
  • Develop, test and support data pipelines for extract, transform, load (ETL) of the source system data to populate datawarehouse/datalake/lakehouse.
  • Develop end user facing dashboards and analytics solutions.
  • Support the operations of the IT systems landscape ensuring system uptime, ETL and other job completion as per schedule, ongoing system changes and enhancements.

Qualifications
  • Post Graduate degree with 8+ years of experience or a Bachelor's degree with 10+ years of experience in development and support of Clinical Operations analytics solutions.
  • Demonstrated strong experience working with developing end user dashboards using solutions such as Qlik, Power BI, Shiny R/Python.
  • Strong Experience developing datalake/lakehouse solutions on platforms such as Snowflake, Databricks, AWS, and Azure.
  • Strong working knowledge of development and management of database technologies such as Postgres, SQLServer etc.
  • Experience with development of data pipelines including ETL from source systems to datawarehouse/datalakes/lakehouse using solutions such as Apache Airflow, Fivetran, dbt etc.
  • Excellent oral and written communication skills with high EQ to effectively collaborate with business cross-functional teams.
  • Understanding of the clinical development lifecycle and demonstrated experience building analytics capabilities in clinical development
  • Knowledge of Report/Dashboard development in Veeva R&D Vaults such Clinical, RIM, Quality, Safety is preferred.
  • Knowledge of IT Computer System Validation (CSV) in a GxP environment is preferred.
  • Experience with Automation and AI Agent Frameworks is preferred.
  • Deep knowledge of RBQM, Quality by Design (QbD) and regulatory/operational expectations for clinical oversight is preferred.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:
  • 401k plan with company matching
  • Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
  • Mental health and wellness benefits
  • Weeklong summer and winter holiday shutdowns
  • Generous paid time off and holiday policies
  • Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
  • Enhanced parental leave benefit
  • Daily subsidized lunch program when on-site

The expected salary range for this role is $191,000 to $209,000 depending on skills, competency, and the market demand for your expertise.
Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.
We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.

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