... 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 ...
... 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 ...
Part Time LCSW-R. Syracuse Jewish Family Services at Menorah Park of CNY Responsibilities include ... programming. Must be comfortable and well-versed in use of telehealth platforms as well as in ...
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Part Time LCSW-R. Syracuse Jewish Family Services at Menorah Park of CNY Responsibilities include ... programming. Must be comfortable and well-versed in use of telehealth platforms as well as in ...
Part Time LCSW-R. Syracuse Jewish Family Services at Menorah Park of CNY Responsibilities include ... programming. Must be comfortable and well-versed in use of telehealth platforms as well as in ...
Part Time LCSW-R. Syracuse Jewish Family Services at Menorah Park of CNY Responsibilities include ... programming. Must be comfortable and well-versed in use of telehealth platforms as well as in ...
Part Time LCSW-R. Syracuse Jewish Family Services at Menorah Park of CNY Responsibilities include ... programming. Must be comfortable and well-versed in use of telehealth platforms as well as in ...
Part Time LCSW-R. Syracuse Jewish Family Services at Menorah Park of CNY Responsibilities include ... programming. Must be comfortable and well-versed in use of telehealth platforms as well as in ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Familiarity with clinical data management concepts * Strategic thinking - ability to turn strategy ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Familiarity with clinical data management concepts * Strategic thinking - ability to turn strategy ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Familiarity with clinical data management concepts * Strategic thinking - ability to turn strategy ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Familiarity with clinical data management concepts * Strategic thinking - ability to turn strategy ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Familiarity with clinical data management concepts * Strategic thinking - ability to turn strategy ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Familiarity with clinical data management concepts * Strategic thinking - ability to turn strategy ...
Associate Director, Clinical and Statistical Programming
$185.10K - $228.70K/yr
POSITION SUMMARY The Associate Director, Statistical Programming will be responsible for strategic ... Experience with using R in clinical analysis Physical Requirements: * Ability to sit for prolonged ...
Associate Director, Clinical and Statistical Programming
$185.10K - $228.70K/yr
POSITION SUMMARY The Associate Director, Statistical Programming will be responsible for strategic ... Experience with using R in clinical analysis Physical Requirements: * Ability to sit for prolonged ...
... Clinical R&D. Summary of Key Responsibilities * Identify, develop, and execute Sourcing Category ... Bachelor's Degree, ideally in Business, Science, Engineering, or Supply Chain. Advanced Degree (MS ...
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... Clinical R&D. Summary of Key Responsibilities * Identify, develop, and execute Sourcing Category ... Bachelor's Degree, ideally in Business, Science, Engineering, or Supply Chain. Advanced Degree (MS ...
Associate Director, Biostatistics
Cambridge, MA · On-site +1
$185.30K - $250.70K/yr
Desired Experience: • Experience in clinical development through Phase 3 (NDA submission). • ... Proficiency in R programming language and other statistical software, including EAST. • ...
Associate Director, Biostatistics
Cambridge, MA · On-site +1
$185.30K - $250.70K/yr
Desired Experience: • Experience in clinical development through Phase 3 (NDA submission). • ... Proficiency in R programming language and other statistical software, including EAST. • ...
Senior Statistical Programmer - Remote
Fairfield, CT · On-site +1
In this role, you will transform raw clinical data into analysis ready datasets, generate high ... CDISC standards expertise; knowledge of additional programming languages (R, Python) is a plus.
Senior Statistical Programmer - Remote
Fairfield, CT · On-site +1
In this role, you will transform raw clinical data into analysis ready datasets, generate high ... CDISC standards expertise; knowledge of additional programming languages (R, Python) is a plus.
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
Programmer
Boston, MA · On-site
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
Programmer
Boston, MA · On-site
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 ...
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 ...
Modeling & Simulations Scientist II - PKPD Programming
Boston, MA · On-site
$124.60K - $187K/yr
Advanced proficiency in R programming and strong understanding of clinical trial data structures, derivations, and traceability . * Solid understanding of quality control, validation practices, and ...
Modeling & Simulations Scientist II - PKPD Programming
Boston, MA · On-site
$124.60K - $187K/yr
Advanced proficiency in R programming and strong understanding of clinical trial data structures, derivations, and traceability . * Solid understanding of quality control, validation practices, and ...
... programming, are also encouraged and available.\r\n\r\nThe duties of a Clinical Social Worker ... within our agency may include:\r\n\r\n Conducting comprehensive mental health assessments\r\n ...
... programming, are also encouraged and available.\r\n\r\nThe duties of a Clinical Social Worker ... within our agency may include:\r\n\r\n Conducting comprehensive mental health assessments\r\n ...
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 ...
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 ...
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 ...
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 ...
Senior Principal Statistical Programmer
$119.70K - $222.30K/yr
SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming. Video Link ...
Senior Principal Statistical Programmer
$119.70K - $222.30K/yr
SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming. Video Link ...
Senior Principal Statistical Programmer
$119.70K - $222.30K/yr
SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming. Video Link ...
Senior Principal Statistical Programmer
$119.70K - $222.30K/yr
SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming. Video Link ...
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
PTO
This job post has expired today. Applications are no longer accepted.
Johnson & Johnson rating
8.1
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 SciencesJob Sub Function:
BiostatisticsJob Category:
People LeaderAll Job Posting Locations:
Irvine, California, United States of AmericaJob 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) ProgrammingThe anticipated base pay range for this position is :
$137,000.00 - $235,750.00Additional 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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