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Clinical R Programmer Jobs in Reading, PA (NOW HIRING)

Occupational Therapist (OT)

Pottsville, PA ยท On-site

$36.75 - $48.50/hr

A.R.E. (Service, Honesty, Accountability, Respect, and Excellence) * An employer who cares about ... Occupational Therapist (OT) will be responsible for Clinical Programming and for maintaining ...

Occupational Therapist (OT)

Pottsville, PA ยท On-site

$36.75 - $48.50/hr

A.R.E. (Service, Honesty, Accountability, Respect, and Excellence) * An employer who cares about ... Occupational Therapist (OT) will be responsible for Clinical Programming and for maintaining ...

Senior Scientist Omics - IMM

Reading, PA ยท On-site

$72K - $99K/yr

... scale clinical, genetic, omics and cell phenotype data to advance our drug discovery and ... Proficient in programming and computational skills and demonstrated ability to work with a group of ...

Clinical R Programmer information

See Reading, PA salary details

$23

$62

$98

How much do clinical r programmer jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for clinical r programmer in Reading, PA is $62.21, according to ZipRecruiter salary data. Most workers in this role earn between $51.49 and $70.43 per hour, depending on experience, location, and employer.

What is a Clinical R programmer?

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 skills and qualifications are needed to be a Clinical R programmer?

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 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 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 Reading, PA?

For Clinical R Programmer jobs in Reading, PA, the most frequently searched job titles are:

What cities near Reading, PA are hiring for Clinical R Programmer jobs?

Cities near Reading, PA with the most Clinical R Programmer job openings:

Infographic showing various Clinical R Programmer job openings in Reading, PA as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $129,389 per year, or $62.2 per hour.

Principal Scientist, Data Science - R&D DDSAI - Therapeutics Development & Supply (TDS)

Johnson and Johnson

Reading, PA โ€ข On-site

Full-time

Retirement, PTO

Posted 8 days ago


Job description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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:
Data Science
Job Category:
Scientific/Technology
All Job Posting Locations:
Madrid, Spain, Malvern, Pennsylvania, United States of America, Spring House, Pennsylvania, United States of America
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for Principal Scientist, Data Science - R&D DDSAI - Therapeutics Development & Supply (TDS)
The primary location for this position is open to Spring House, PA; Malvern, PA; Madrid, Spain
J&J Innovative Medicine develops treatments that improve the health of people worldwide. Research and development areas encompass oncology, immunology, neuroscience, cardiopulmonary and specialty ophthalmology. Our goal is to help people live longer, healthier lives. We have produced and marketed many first-in-class prescription medications and are poised to serve the broad needs of the healthcare market - from patients to practitioners and from clinics to hospitals. To learn more about Johnson & Johnson Innovative Medicine visit https://innovativemedicine.jnj.com/
POSITION SUMMARY
The R&D Data, Data Science and AI organization is seeking a Data Scientist - Data Engineer to design, build, and optimize data capture, processing, and storage solutions that enable advanced analytics, digital process transformation, and AI/ML applications across the development-to-supply continuum for Therapeutics Development & Supply (TDS).
You will be a hands-on technical contributor working across Process Development, Manufacturing, Supply Chain, Quality, and Digital/Data Science teams to deliver high-quality, AI-ready data pipelines and data products. This role involves creating robust, future-proof data systems, engineering workflows, and high-value data repositories that support scientific, technical, and operational decision-making.
KEY RESPONSIBILITIES
Data Engineering & Pipeline Development
  • Design, build, and maintain scalable data pipelines for acquiring, integrating, and managing TDS data from diverse data generation sources and systems (e.g., lab systems, MES, clinical supply, quality systems, external partners).
  • Create and optimize data flows for structured and unstructured data using Python, R, SQL, DBT, cloud services, and other modern engineering tools.
  • Develop and maintain TDS-specific data repositories, implementing enterprise-level data models and creating new models as needed.
  • Enable AI/ML readiness by ensuring data is well-structured, versioned, traceable, and semantically aligned with enterprise data standards.

Data Product & Architecture Partnership
  • Partner with data scientists, TDS domain experts, and digital technology teams to translate business needs into high-quality data products and engineering requirements.
  • Work closely with ontology/knowledge graph teams to implement semantic models and future-proof data architectures.

Quality, Compliance & Performance
  • Implement data quality and performance standards; define KPIs to measure accuracy, completeness, and consistency across TDS data assets.
  • Apply data versioning and lineage tracking for compliance, traceability, and audit readiness.
  • Follow software development best practices including code versioning, DevOps integration, and documentation.

Cross-Functional Collaboration
  • Engage with scientific, technical, and operations stakeholders to understand requirements, design data solutions, and drive adoption.
  • Support multiple concurrent projects, managing priorities and delivering maximum business value across the TDS network.

QUALIFICATIONS
Required
  • Advanced degree in Engineering, Data Science, Life Sciences, Computer Science, or related field; advanced degree preferred.
  • 3+ years of experience in data engineering, including data modeling and database design, preferably in a scientific, manufacturing, or healthcare environment.
  • Proficiency with Python, R, SQL, and cloud-based architectures (e.g., AWS services, Snowflake, Redshift).
  • Experience with NoSQL and graph databases.
  • Strong analytical, problem-solving, and stakeholder-management skills, with the ability to translate discussions into actionable requirements.
  • Ability to drive multiple exciting projects simultaneous with strong organizational skills and adaptability.

Preferred
  • Experience with regulated or standards-driven data environments, such as CDISC, HL7, FHIR, OMOP, DICOM, or manufacturing/quality data standards.
  • Familiarity with high-dimensional data (e.g., imaging, sensor data, etc).
  • Experience with principles connecting to or feeding MLOps and model deployment workflows.
  • Knowledge of manufacturing systems (MES), laboratory information systems, or industrial data systems.
  • Experience with knowledge graph architectures.

Why This Role Is Unique
This is a rare opportunity to grow in one of the world's most ambitious and fast growing R&D Data Science organizations, shaping how Therapeutics Development & Supply data powers next-generation therapies in the largest biomedical company on the planet. Your work will directly accelerate Johnson & Johnson's scientific discovery, fuel AI innovation, and impact patients globally.
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.
#JRDDS
#JNJDataScience
JNJIMRND-DS
Required Skills:
Preferred Skills:
Advanced Analytics, Coaching, Critical Thinking, Data Analysis, Data Privacy Standards, Data Quality, Data Reporting, Data Savvy, Data Science, Data Visualization, Digital Fluency, Econometric Models, Organizing, Process Improvements, Strategic Thinking, Technical Credibility, Workflow Analysis
The anticipated base pay range for this position is :
$117,000.00 - $201,250.00
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company's long-term incentive program.
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