We are seeking a Clinical R programmer / Principal Clinical Data Scientist to join our Scientific Computing Technology group, which builds the open-source tools, R packages, SAS macros, and computing ...
We are seeking a Clinical R programmer / Principal Clinical Data Scientist to join our Scientific Computing Technology group, which builds the open-source tools, R packages, SAS macros, and computing ...
IQVIA is a leading global provider of clinical research services, commercial insights and health ... They are seeking an experienced R programmer to provide technical expertise for the clinical PK/PD ...
IQVIA is a leading global provider of clinical research services, commercial insights and health ... They are seeking an experienced R programmer to provide technical expertise for the clinical PK/PD ...
Principal R Programmer
$98.20K - $273.20K/yr
Experienced R programmer needed to provide technical expertise for clinical PK/PD department to meet internal and external needs. Uses R and companion software to develop custom programming code to ...
Principal R Programmer
$98.20K - $273.20K/yr
Experienced R programmer needed to provide technical expertise for clinical PK/PD department to meet internal and external needs. Uses R and companion software to develop custom programming code to ...
Principal R Programmer
$98.20K - $273.20K/yr
Experienced R programmer needed to provide technical expertise for clinical PK/PD department to meet internal and external needs. Uses R and companion software to develop custom programming code to ...
Principal R Programmer
$98.20K - $273.20K/yr
Experienced R programmer needed to provide technical expertise for clinical PK/PD department to meet internal and external needs. Uses R and companion software to develop custom programming code to ...
Principal R Programmer
Durham, NC · On-site
$98.20K - $273.20K/yr
Experienced R programmer needed to provide technical expertise for clinical PK/PD department to meet internal and external needs. Uses R and companion software to develop custom programming code to ...
Principal R Programmer
Durham, NC · On-site
$98.20K - $273.20K/yr
Experienced R programmer needed to provide technical expertise for clinical PK/PD department to meet internal and external needs. Uses R and companion software to develop custom programming code to ...
Sr R & SAS Programmer
Chesterbrook, PA · On-site
Knowledge of R programming in clinical trials Familiarity of the drug development process. Knowledge of CDISC standards and electronic submission requirements. Strong SAS and SAS Macro language ...
Sr R & SAS Programmer
Chesterbrook, PA · On-site
Knowledge of R programming in clinical trials Familiarity of the drug development process. Knowledge of CDISC standards and electronic submission requirements. Strong SAS and SAS Macro language ...
... of chemistry, engineering, computation, and biology to discover novel treatments for life ... Clinical R&D. * Design and implementation of datawarehouse/datalake/lakehouse including star ...
... of chemistry, engineering, computation, and biology to discover novel treatments for life ... Clinical R&D. * Design and implementation of datawarehouse/datalake/lakehouse including star ...
Senior Clinical Programmer
Cambridge, MA · On-site +1
Proficient in clinical data programming languages (e.g., SAS, R, SQL, etc.). * Expertise in clinical programming platforms, including experience with clinical data workflows, data integration, and ...
Senior Clinical Programmer
Cambridge, MA · On-site +1
Proficient in clinical data programming languages (e.g., SAS, R, SQL, etc.). * Expertise in clinical programming platforms, including experience with clinical data workflows, data integration, and ...
Build and maintain R-based analytical environments for clinical and outcomes research * Design and ... Solid software engineering fundamentals (version control, testing, CI/CD) Work Authorization ...
Quick apply
Build and maintain R-based analytical environments for clinical and outcomes research * Design and ... Solid software engineering fundamentals (version control, testing, CI/CD) Work Authorization ...
Platform Engineer, Statistical Computing (R)
$180K - $220K/yr
Build and maintain R-based analytical environments for clinical and outcomes research > * Design ... Solid software engineering fundamentals (version control, testing, CI/CD) > Work Authorization ...
Platform Engineer, Statistical Computing (R)
$180K - $220K/yr
Build and maintain R-based analytical environments for clinical and outcomes research > * Design ... Solid software engineering fundamentals (version control, testing, CI/CD) > Work Authorization ...
Clinical SAS Programmer
Chantilly, VA · Remote
Clinical SAS Programmer No of positions- 2 Location- Remote Experience Required:6+ Years Education ... Experience with R and Python is a strong plus. * Ability to work independently and collaboratively ...
Quick apply
Clinical SAS Programmer
Chantilly, VA · Remote
Clinical SAS Programmer No of positions- 2 Location- Remote Experience Required:6+ Years Education ... Experience with R and Python is a strong plus. * Ability to work independently and collaboratively ...
Psychologist (Clinical)
$89.60K - $123.50K/yr
... Clinical)to join our mental healthcare team at theAlbert J. Solnit Psychiatric Center - South ... programming, are also encouraged and available.\r\n\r\nMore details about this role can be found in ...
Psychologist (Clinical)
$89.60K - $123.50K/yr
... Clinical)to join our mental healthcare team at theAlbert J. Solnit Psychiatric Center - South ... programming, are also encouraged and available.\r\n\r\nMore details about this role can be found in ...
Responsibilities As a Statistical Programming Consultant, you will use your SAS and R programming ... At least 6 years of Clinical trials related work experience in SAS programming, analysis and ...
Responsibilities As a Statistical Programming Consultant, you will use your SAS and R programming ... At least 6 years of Clinical trials related work experience in SAS programming, analysis and ...
R programming skils in clinical trials * Strong knowledge of industry standards. * Ability to work on data integrations (ISS and ISE). * Strong oral and written communication skills. Ability to ...
R programming skils in clinical trials * Strong knowledge of industry standards. * Ability to work on data integrations (ISS and ISE). * Strong oral and written communication skills. Ability to ...
Senior Manager, Clinical Statistical Programmer
$140K - $198K/yr
This role combines deep technical expertise in SAS and R with ownership of ongoing safety ... Lead Statistical Programming processes, support Clinical strategies, and manage the execution of ...
Quick apply
Senior Manager, Clinical Statistical Programmer
$140K - $198K/yr
This role combines deep technical expertise in SAS and R with ownership of ongoing safety ... Lead Statistical Programming processes, support Clinical strategies, and manage the execution of ...
Senior Manager, Clinical Statistical Programmer
Boston, MA · On-site
$140K - $198K/yr
This role combines deep technical expertise in SAS and R with ownership of ongoing safety ... Lead Statistical Programming processes, support Clinical strategies, and manage the execution of ...
Senior Manager, Clinical Statistical Programmer
Boston, MA · On-site
$140K - $198K/yr
This role combines deep technical expertise in SAS and R with ownership of ongoing safety ... Lead Statistical Programming processes, support Clinical strategies, and manage the execution of ...
Extensive experience with clinical data systems (particularly Medidata Rave) and languages like SAS, R or Python * Proven experience in clinical trial programming and database management * Knowledge ...
Extensive experience with clinical data systems (particularly Medidata Rave) and languages like SAS, R or Python * Proven experience in clinical trial programming and database management * Knowledge ...
... clinical trial analysis Knowledge of Good Programming Practices and GCP Preferred Experience with R programming Additional Requirements Hands-on experience with LSAF - Life Sciences Analytical ...
... clinical trial analysis Knowledge of Good Programming Practices and GCP Preferred Experience with R programming Additional Requirements Hands-on experience with LSAF - Life Sciences Analytical ...
Excellent hands on experience on SAS or R programming language for data review listings/tracker ... Clinical affairs terminology Knowledge of Good Clinical Practices, Clinical research, Clinical ...
Excellent hands on experience on SAS or R programming language for data review listings/tracker ... Clinical affairs terminology Knowledge of Good Clinical Practices, Clinical research, Clinical ...
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.
Quick apply
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.
Clinical R Programmer information
See salary details
$24.76 - $31.84
3% of jobs
$31.84 - $38.92
4% of jobs
$38.92 - $46
9% of jobs
$46 - $53.08
5% of jobs
$54.30 is the 25th percentile. Wages below this are outliers.
$53.08 - $60.16
17% of jobs
The median wage is $63.26 / hr.
$60.16 - $67.24
25% of jobs
$71.78 is the 75th percentile. Wages above this are outliers.
$67.24 - $74.32
17% of jobs
$74.32 - $81.40
9% of jobs
$81.40 - $88.48
6% of jobs
$88.48 - $95.56
2% of jobs
$95.56 - $102.64
1% of jobs
$24
$64
$102
How much do clinical r programmer jobs pay per hour?
What are the key skills and qualifications needed to thrive as a Clinical R Programmer, and why are they important?
What are some common challenges faced by Clinical R Programmers when working with clinical trial data?
What are Clinical R Programmers?
What is the difference between Clinical R Programmer vs Clinical SAS Programmer?
| 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.

Full-time
Posted 11 days ago
Job description
ClinChoice is searching for a Principal Clinical Data Scientist Consultant - R Programmer to join one of our clients.
We are seeking a Clinical R programmer / Principal Clinical Data Scientist to join our Scientific Computing Technology group, which builds the open-source tools, R packages, SAS macros, and computing systems that power clinical programming, data management, and biostatistics across the organization. Reporting to the Director of Statistical Programming, this role blends hands-on clinical deliverables with contributions to the open-source and internal tooling that supports the wider clinical technical community. The ideal candidate has strong R skills, deep clinical programming experience, working Python familiarity, and an interest in modern, reproducible workflows. This position is open to remote candidates.
Key Responsibilities
- Develop, validate, and maintain SDTM and ADaM datasets in R - using admiral and the broader pharmaverse - following CDISC standards.
- Generate Tables, Listings, and Figures (TLFs) in R or SAS as required by study needs.
- Perform Pinnacle21 validation, resolve findings, and refine specifications to ensure CDISC compliance and submission readiness.
- Write efficient, reproducible, well-structured R code for clinical data analysis and reporting.
- Contribute to open-source and internal tooling - including R Shiny / teal modules, R packages, SAS macros, and Python utilities - used by clinical programming, data management, and biostatistics teams.
- Partner with statisticians, data managers, and clinical teams to translate programming requirements into reliable deliverables.
- Perform QC, reconcile data issues, and ensure outputs meet regulatory expectations (e.g., FDA, EMA).
- Support automation, pipeline development, and version-controlled workflows.
- Use SAS for legacy studies or where SAS support is needed.
- Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related field.
- 5+ years in clinical programming, with a strong focus on R.
- Proven experience producing SDTM and ADaM datasets in R, including hands-on use of admiral.
- Experience with Pinnacle21 validation and remediation.
- Working knowledge of SAS programming.
- Working knowledge of Python for analytics, scripting, or tooling.
- Solid understanding of CDISC standards (SDTM, ADaM) and metadata-driven programming.
- Experience with clinical trial data, regulatory submissions, and QC processes.
- Strong analytical, problem-solving, and documentation skills.
- Broader pharmaverse experience (e.g., tidyCDISC, rtables) and tidyverse fluency.
- Experience building or contributing to R Shiny apps, teal modules, or R packages used by other teams.
- Exposure to AI/ML tooling in a clinical or programming context.
- Real-World Evidence (RWE) experience - e.g., mapping Flatiron or claims/EHR data into CDISC-aligned structures.
- R Markdown, Quarto, or other reproducible reporting workflows.
- GxP validation, Git-based version control, and CI/CD or automated workflows.
- CRO or pharmaceutical industry experience.
The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we have received it. If you have the requirements we need, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset, and they are the fulcrum around which all ClinChoice activities are built, and close management and training are the core instruments to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our low industry-average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent, guided by a commitment to diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
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About ClinChoice
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Fort Washington, PA, US
Year founded
1995