Clinical Programmer II
Palo Alto, CA · On-site
This role requires strong proficiency in R and/or SAS and understanding of clinical trial processes ... Conduct programming peer reviews, provide technical guidance, and mentor junior programmers to ...
Palo Alto, CA · On-site
This role requires strong proficiency in R and/or SAS and understanding of clinical trial processes ... Conduct programming peer reviews, provide technical guidance, and mentor junior programmers to ...
Palo Alto, CA · On-site
This role requires strong proficiency in R and/or SAS and understanding of clinical trial processes ... Conduct programming peer reviews, provide technical guidance, and mentor junior programmers to ...
Pleasanton, CA · On-site
$140K - $181K/yr
Design, develop, and validate compound-level SAS macros to standardize and automate clinical ... Translate Statistical Analysis Plans into executable SAS/R code to generate regulatory submission ...
Pleasanton, CA · On-site
$140K - $181K/yr
Design, develop, and validate compound-level SAS macros to standardize and automate clinical ... Translate Statistical Analysis Plans into executable SAS/R code to generate regulatory submission ...
... SAS, R, or Stata to work with electronic medical records and claims data. The ultimate aim is to ... The Clinical Data Research Consultants group's services include the administration of Data Use ...
... SAS, R, or Stata to work with electronic medical records and claims data. The ultimate aim is to ... The Clinical Data Research Consultants group's services include the administration of Data Use ...
... R, as well as performing quality reviews of deliverables, both for in-house analyses and outsourced programming tasks. This position serves as a critical bridge between Biostatistics and Clinical ...
... R, as well as performing quality reviews of deliverables, both for in-house analyses and outsourced programming tasks. This position serves as a critical bridge between Biostatistics and Clinical ...
San Jose, CA · On-site +1
The clinical trials may be of moderate scope and complexity. Use programming knowledge to develop ... as R or SAS, is required. * 3+ years of experience of relevant experience in programming is ...
San Jose, CA · On-site +1
The clinical trials may be of moderate scope and complexity. Use programming knowledge to develop ... as R or SAS, is required. * 3+ years of experience of relevant experience in programming is ...
Milpitas, CA · On-site +1
The clinical trials may be of moderate scope and complexity. Use programming knowledge to develop ... as R or SAS, is required. * 3+ years of experience of relevant experience in programming is ...
Milpitas, CA · On-site +1
The clinical trials may be of moderate scope and complexity. Use programming knowledge to develop ... as R or SAS, is required. * 3+ years of experience of relevant experience in programming is ...
Redwood City, CA · On-site
$183K - $269K/yr
... of clinical data, and global submission requirements * Proficiency with statistical programming in SAS. Familiarity with SAS/GRAPH, SAS/MACRO, and R * Demonstrated ability to apply complex ...
Redwood City, CA · On-site
$183K - $269K/yr
... of clinical data, and global submission requirements * Proficiency with statistical programming in SAS. Familiarity with SAS/GRAPH, SAS/MACRO, and R * Demonstrated ability to apply complex ...
$120K - $175K/yr
Supira Medical, a clinical-stage Shifamed Portfolio Company, is developing a low-profile, high ... Work closely with the company's R amp;D Engineers to obtain latest product change and identify ...
$120K - $175K/yr
Supira Medical, a clinical-stage Shifamed Portfolio Company, is developing a low-profile, high ... Work closely with the company's R amp;D Engineers to obtain latest product change and identify ...
Palo Alto, CA · On-site +1
$180K/yr
Proven experience as a lead programmer for clinical trials and complex technical projects ... Familiarity with other programming languages or tools (e.g., R , Python , Git , VB ) is a plus.
Palo Alto, CA · On-site +1
$180K/yr
Proven experience as a lead programmer for clinical trials and complex technical projects ... Familiarity with other programming languages or tools (e.g., R , Python , Git , VB ) is a plus.
Palo Alto, CA · On-site
$180K/yr
Proven experience as a lead programmer for clinical trials and complex technical projects ... Familiarity with other programming languages or tools (e.g., R , Python , Git , VB ) is a plus.
Palo Alto, CA · On-site
$180K/yr
Proven experience as a lead programmer for clinical trials and complex technical projects ... Familiarity with other programming languages or tools (e.g., R , Python , Git , VB ) is a plus.
Palo Alto, CA · On-site
$180K/yr
Proven experience as a lead programmer for clinical trials and complex technical projects ... Familiarity with other programming languages or tools (e.g., R , Python , Git , VB ) is a plus.
Quick apply
Palo Alto, CA · On-site
$180K/yr
Proven experience as a lead programmer for clinical trials and complex technical projects ... Familiarity with other programming languages or tools (e.g., R , Python , Git , VB ) is a plus.
Our clinical research efforts employ new techniques for deep phenotyping, such as deep learning ... Demonstrated fluency and competency with statistical programming with the R programming language or ...
Our clinical research efforts employ new techniques for deep phenotyping, such as deep learning ... Demonstrated fluency and competency with statistical programming with the R programming language or ...
Proficiency and experience programming using R and/or Python. * Proficiency in statistical models and analysis of clinical data. Some ML experience a strong plus. * Proficiency in visualizations and ...
Proficiency and experience programming using R and/or Python. * Proficiency in statistical models and analysis of clinical data. Some ML experience a strong plus. * Proficiency in visualizations and ...
Hayward, CA · On-site
$245 - $260/hr
An advanced degree in Pharmaceutics/Pharmacy/Engineering/Statistics with demonstrated expertise in ... Expertise with standard modelling and simulation software (NONMEM, S‑Plus/R, etc) is required.
Hayward, CA · On-site
$245 - $260/hr
An advanced degree in Pharmaceutics/Pharmacy/Engineering/Statistics with demonstrated expertise in ... Expertise with standard modelling and simulation software (NONMEM, S‑Plus/R, etc) is required.
Demonstrated proficiency in statistical programming (R and/or SAS), with the ability to ... Experience overseeing clinical data management and systems (EDC, CDISC standards, analytics ...
Demonstrated proficiency in statistical programming (R and/or SAS), with the ability to ... Experience overseeing clinical data management and systems (EDC, CDISC standards, analytics ...
Brisbane, CA · On-site
$245 - $260/hr
An advanced degree in Pharmaceutics, Pharmacy, Engineering or Statistics with demonstrated ... Expertise with standard modelling and simulation software (NONMEM, S‑Plus/R, etc.) is required.
Brisbane, CA · On-site
$245 - $260/hr
An advanced degree in Pharmaceutics, Pharmacy, Engineering or Statistics with demonstrated ... Expertise with standard modelling and simulation software (NONMEM, S‑Plus/R, etc.) is required.
Redwood City, CA · On-site
$132K - $226K/yr
This role sits at the intersection of data science and clinical research, requiring expertise in data cleaning, transformation, and statistical programming (R, Python, SQL) to generate reports and ...
Redwood City, CA · On-site
$132K - $226K/yr
This role sits at the intersection of data science and clinical research, requiring expertise in data cleaning, transformation, and statistical programming (R, Python, SQL) to generate reports and ...
Redwood City, CA · On-site
$132K - $226K/yr
This role sits at the intersection of data science and clinical research, requiring expertise in data cleaning, transformation, and statistical programming (R, Python, SQL) to generate reports and ...
Redwood City, CA · On-site
$132K - $226K/yr
This role sits at the intersection of data science and clinical research, requiring expertise in data cleaning, transformation, and statistical programming (R, Python, SQL) to generate reports and ...
Brisbane, CA · On-site
$245K - $260K/yr
An advanced degree in Pharmaceutics/Pharmacy/Engineering/Statistics with demonstrated expertise in ... Expertise with standard modelling and simulation software (NONMEM, S-Plus/R, etc) is required.
Brisbane, CA · On-site
$245K - $260K/yr
An advanced degree in Pharmaceutics/Pharmacy/Engineering/Statistics with demonstrated expertise in ... Expertise with standard modelling and simulation software (NONMEM, S-Plus/R, etc) is required.
Proficiency and experience programming using R and/or Python. * Proficiency in statistical models and analysis of clinical data. Some ML experience a strong plus. * Proficiency in visualizations and ...
Proficiency and experience programming using R and/or Python. * Proficiency in statistical models and analysis of clinical data. Some ML experience a strong plus. * Proficiency in visualizations and ...
$29.21 - $37.56
3% of jobs
$37.56 - $45.91
4% of jobs
$45.91 - $54.27
9% of jobs
$54.27 - $62.62
5% of jobs
$64.05 is the 25th percentile. Wages below this are outliers.
$62.62 - $70.97
17% of jobs
The median wage is $74.63 / hr.
$70.97 - $79.32
25% of jobs
$84.67 is the 75th percentile. Wages above this are outliers.
$79.32 - $87.68
17% of jobs
$87.68 - $96.03
9% of jobs
$96.03 - $104.38
6% of jobs
$104.38 - $112.73
2% of jobs
$112.73 - $121.09
1% of jobs
$29
$76
$121
| Aspect | Clinical R Programmer | Clinical SAS Programmer |
|---|---|---|
| Required Credentials | Typically requires a degree in statistics, biostatistics, or related field; proficiency in R programming | Usually requires a degree in statistics, biostatistics, or related field; proficiency in SAS programming |
| Work Environment | Often works in research-focused settings, academia, or biotech companies using open-source tools | Commonly employed in pharmaceutical companies, CROs, and clinical trial data analysis using SAS |
| Industry Usage | Growing in popularity for data analysis and visualization in clinical research | Standard 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.
At Recor Medical, we are pioneering Ultrasound Renal Denervation (uRDN) therapy to treat hypertension, the leading cardiovascular risk factor in the world. With our Paradise uRDN System, we're on a mission to provide the millions of people who suffer from hypertension with a non-drug and minimally invasive option to lower their blood pressure. Join us on our journey and make a meaningful impact on the lives of people around the globe.
Position Summary
The Clinical Programmer II at Recor Medical develops and maintains advanced programming solutions for clinical trial data management, analysis, and reporting. This role requires strong proficiency in R and/or SAS and understanding of clinical trial processes and operational metrics. Key responsibilities include performing complex data analysis, generating reports, and creating tools to support both clinical research and operational decision-making. The ideal candidate will collaborate with cross-functional teams, mentor junior programmers, and contribute to process improvements. They will demonstrate technical expertise, problem-solving skills, and the ability to work independently and collaboratively, while staying current with industry trends and maintaining high standards of quality and compliance.
Responsibilities and Duties
Design, develop, validate, and maintain complex programs to support clinical trial data management processes, including data integration, transformation, and analysis using R, SAS, or other relevant programming languages.
Perform advanced data analysis and generate complex reports, tables, listings, and figures to support clinical trial data review, statistical analysis, regulatory submissions, and operational decision-making.
Support clinical operational activities by developing and maintaining tools for tracking study progress, site performance, and other key operational metrics, including generating regular reports and dashboards to provide insights into clinical trial operations.
Collaborate with cross-functional teams to implement statistical analysis plans and design programming solutions that address specific project requirements.
Troubleshoot complex data issues and propose solutions to ensure data integrity and quality throughout the clinical development process.
Conduct programming peer reviews, provide technical guidance, and mentor junior programmers to ensure code quality and adherence to standards.
Participate in version control using Git and maintain comprehensive documentation for scripts, packages, and applications.
Contribute to the development of study documentation, including programming specifications and data management plans.
Lead process improvement initiatives to enhance efficiency and quality in clinical programming activities.
Stay abreast of emerging trends, technologies, and industry standards (e.g., CDISC) in clinical programming and data management, implementing improvements as appropriate and assisting in preparing for regulatory audits and inspections.
Other duties as assigned
Requirements
Master's degree in computer science, data science, statistics, life sciences, or related field with 1+ years of experience; or a Bachelor's degree in these fields with 2+ years of professional experience in Clinical Programming, data visualization, business intelligence, or analytics roles.
Strong proficiency in R and/or SAS, with experience in other relevant programming languages and tools (e.g., Python, SQL).
Demonstrated ability to identify and resolve performance bottlenecks and optimize code for efficiency and scalability.
Experience in extracting, cleaning, transforming, and loading data from diverse sources, managing datasets, and ensuring data quality and integrity.
Understanding of clinical trial processes and data flow from study setup to database lock.
Working knowledge of clinical trial data standards (e.g., CDISC SDTM, ADaM) is strongly preferred.
Experience with or understanding of clinical trial operations and associated metrics is highly desirable.
Excellent problem-solving and analytical skills, with the ability to translate complex requirements into efficient programming solutions.
Experience with version control systems (e.g., Git) and collaborative development practices.
Familiarity with tools and techniques for visualizing operational data and creating interactive dashboards (e.g., Tableau, Power BI) is a plus.
Ability to mentor junior team members, including conducting code reviews and providing technical guidance.
Strong written and verbal communication skills, with the ability to explain technical concepts to non-technical stakeholders.
Demonstrated ability to work independently and collaboratively in a fast-paced environment.
Commitment to continuous learning and staying updated with emerging trends in clinical programming and data analysis.
Preferred Skills
Experience with data visualization tools (e.g., Power BI, Tableau)
Proficiency in version control systems (e.g., Git) and collaborative development practices
Experience mentoring junior programmers and conducting code reviews
Familiarity with cloud-based data platforms and integration technologies
Experience with software validation per FDA guidelines
Knowledge of machine learning or advanced analytics techniques applicable to clinical data
Salary range: $122,8567 - $132,796 (Annual Base Salary)
The successful candidate's starting base pay will be determined based on job-related skills, experience, qualifications, work location and market conditions. The expected base pay range for this role may be modified based on market conditions.
Equal Employment Opportunity
At Recor Medical, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.
Pre-Employment Requirements
At Recor Medical, patient safety, integrity, and regulatory compliance are foundational to everything we do. To support these standards,employmentis contingent upon meeting the following requirements:
Radiation Safety Requirement
Certain field-based roles at Recor Medical require work in environments where radiation sources (e.g., x-ray equipment) are in use. Employees in these roles will be issued a personal dosimetry badge to monitor occupational exposure and are required to wear it in accordance with company policy and applicable regulatory standards. This program is designed to ensure compliance with federal and state regulations and to maintain radiation exposure at levels that are As Low As Reasonably Achievable (ALARA). Additional guidance and protective equipment, as necessary, will be provided as part of onboarding and ongoing safety training.
Respecting your privacy is an essential part of the Company's privacy program and we are committed to the proper handling of Personal Information collected or processed in connection with an Applicant's application for employment, a Contract Worker's work, or a Former Employee's employment at Recor. Refer to our Applicant, Contract Worker & Former Employee Privacy Policy for more detail information.
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Medical equipment and supplies manufacturing
11 - 50 Employees
Palo Alto, CA, US
2009