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Clinical R Programmer Jobs (NOW HIRING)

Our 70+ faculty are leaders in the development of statistical methods for clinical trials and ... Maintain databases using R, Python, and SQL in collaboration with members of the research team

Our 70+ faculty are leaders in the development of statistical methods for clinical trials and ... Maintain databases using R, Python, and SQL in collaboration with members of the research team

Senior Statistical Programmer

Irvine, CA · On-site

$75 - $98.48/hr

R * Provide hands on statistical programming support for clinical studies, including development and validation of analysis datasets and statistical outputs, in accordance with regulatory and company ...

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 ...

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 ...

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Clinical R Programmer information

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$24

$64

$102

How much do clinical r programmer jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for clinical r programmer in the United States is $64.77, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $73.32 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.

More about Clinical R Programmer jobs
What cities are hiring for Clinical R Programmer jobs? Cities with the most Clinical R Programmer job openings:
What states have the most Clinical R Programmer jobs? States with the most job openings for Clinical R Programmer jobs include:
Infographic showing various Clinical R Programmer job openings in the United States as of May 2026, with employment types broken down into 76% Full Time, 14% Part Time, and 10% Contract. Highlights an 71% In-person, and 29% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

Associate Director of Stats Programming

Johnson & Johnson

Irvine, CA • On-site

Full-time

PTO

This job post has expired today. Applications are no longer accepted.


Johnson & Johnson rating

8.1

Company rating: 8.1 out of 10

Based on 99 frontline employees who took The Breakroom Quiz

33rd of 71 rated pharmaceutical


Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Data Analytics & Computational Sciences

Job Sub Function:

Biostatistics

Job Category:

People Leader

All Job Posting Locations:

Irvine, California, United States of America

Job Description:

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that's reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for the best talent for an Associate Director of Stats Programming to support our Electrophysiology business. This role will work onsite in our Irvine, CA office, following hybrid schedule.

OVERALL RESPONSIBILITIES:

The Programming Leader will lead a team ofSAS and R programmers in the Medical Devices Sector. This individual will be accountable for the programming of statisticaldeliverables for pre- and post-market global clinical trials across all Franchises. S/he ensures that programmed datasets, tables, reports and listings are accurate, while meeting timelines and budgets.

POSITION DUTIES & RESPONSIBILITIES:

Reporting to the Sr. Director, Biostatistics and Data Management, this individual will;

  • Provide leadership and direction for Programming by establishing programming standards, and mentoring and managing staff
  • Implement and maintain SAS and R platforms that will allow efficient allocation of programming resources
  • Develop and maintain global SAS macro and R function libraries.
  • Work withData Management leadership to provide input on data and process standards
  • Provide oversight of all programming deliverablesfor clinical trials
  • Develop and maintain global harmonized processes and proceduresfor programming
  • Lead vendor evaluation, selection, contracting, and oversight activities for studies where programming is outsourced to a CRO
  • Work with Clinical Data Science partners, and leadershipin Clinical Operations and Franchise toset priorities and develop project management plans for trial execution including timelines, milestones, and budgets
  • Provide oversight of the quality review of all programming deliverables
  • Know and follow all laws and policies that apply to the job, and maintain the highest levels of professionalism, ethics and compliance at all times
  • Diligently participate in compliance program-related activities as denoted by the supervisor or Chief Compliance Officer
  • Performs other related duties as required.

Functional and Technical Competencies:

  • Demonstrated ability to lead teams to deliver critical milestones.
  • Strong proficiency in Base SAS, SAS/STAT and SAS Macro language. Advanced SAS certification preferred.
  • Strong proficiency in R, advanced R programming preferred.
  • Experience with CDISC datasets, tables, listings and figures preferred;
  • Excellent verbal and written communication skills

Leadership Competencies:

  • Connect - Develop strategic partnerships with key internal stakeholders and external experts to lead implementation of industry programming standards
  • Shape - Develop knowledge of therapeutic areas within the Franchises and adapt ADaM and STDM standards for medical devices for use in the MD sector

Lead - build and develop talent through change to provide high quality programming capability

  • Deliver - ensure high quality programming deliverables for clinical programs are delivered on time, within budget and in compliance to regulations and SOPs, seamlessly across all Franchises

EDUCATION & EXPERIENCE REQUIREMENTS:

  • A Bachelor's degree in Statistics, Computer Science or related discipline, with at least 8 years of programming experience in clinical research within Medical Device or Pharmaceuticals, and at least 3 years of supervisory experience.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers. Internal employees contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

Advanced Analytics, Biostatistics, Collaborating, Compliance Management, Courage, Critical Thinking, Data Privacy Standards, Data Synthesis, Data Visualization, Developing Others, Good Clinical Practice (GCP), Inclusive Leadership, Leadership, Program Management, Quality Assurance (QA), Regulatory Affairs Management, Standard Operating Procedure (SOP), Statistical Analysis Systems (SAS) Programming

The anticipated base pay range for this position is :

$137,000.00 - $235,750.00

Additional Description for Pay Transparency:

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation -120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year
Holiday pay, including Floating Holidays -13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave - 80 hours in a 52-week rolling period10 days
Volunteer Leave - 32 hours per calendar year
Military Spouse Time-Off - 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

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