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Added 1 day ago
Principal Statistical Programmer
Immunome, Inc.
Remote, United States
As a Principal Statistical Programmer, you will serve as a senior technical expert within the individual contributor career track. You will independently develop, validate, document, and…
Added 1 day ago
GL
Principal Programmer
GlaxoSmithKline LLC
Upper Providence, PA
- $126,225 to $210,375 USD / year
…Find out more:Our approach to R&DJob Purpose We are seeking a Principal Programmer to join our Clinical Programming team, contributing to pipeline delivery across complex and pivotal…
Added 1 day ago
Principal Statistical Programmer Consultant – Oncology (Solid Tumors)-Remote
ClinChoice
United States
ClinChoice is searching for a Principal Statistical Programmer Consultant to join one of our clients.
Added 1 day ago
Principal Statistical Programmer FSP - RWD/EPI
Cytel
Washington, DC
Programming and conducting statistical analysis under the direction and supervision of epidemiologists/statisticians including data coding, creation of algorithms, linkage of datasets, and…
Added 2 days ago
Principal Statistical Programmer FSP - RWD/EPI
Jobgether
Remote, United States
…all applications and next steps. Our partner is looking for a Principal Statistical Programmer FSP – RWD/EPI based in United States…
Added 3 days ago
Associate Principal Scientist Statistical Programming, Submission Data Standards Quality Management (Hybrid)
Merck
Rahway, NJ
The Associate Principal Statistical Programmer, Submission Data Standards Quality Management (SDS QM), provides oversight and quality management of submission data standard deliverables for…
Added 10 days ago
Principal Clinical Programmer - RBQM / FSP
IQVIA
Durham, NC
We are seeking a Principal Statistical Programmer to provide full end‑to‑end statistical programming support across clinical development programs. This role requires deep technical…
Added 10 days ago
Senior Principal Statistical Programmer
WCG Clinical
Remote, United States
The Senior Principal Statistical Programmer serves as a senior technical leader and subject matter expert in statistical programming, with deep expertise supporting clinical trials and Data…
Added 14 days ago
NL
Senior Bioinformatics Programmer
NYU Langone Medical Center
New York, NY
- $90,000 to $115,000 USD / year
The Petljak Lab is seeking a highly motivated and creative Senior Bioinformatics Programmer to join our multidisciplinary team within the newly established Cancer Genomics & Genetics…
Added 16 days ago
Principal C&SP Methodology Lead
J&J Family of Companies
Trenton, NJ
The Principal C&SP Methodology Lead is a highly experienced technical programmer/developer with an in-depth understanding of clinical and/or statistical programming processes, tools,…
Added 17 days ago
Senior Research SAS Programmer/Analyst
The Brigham and Women's Hospital, Inc.
United States
The Senior Research Programmer/Analyst will support this mission as part of a highly collaborative multidisciplinary research environment comprising approximately 30 Harvard Medical School…
Added 17 days ago
Senior Research Programmer/Analyst Pharmacoepidemiology
The Brigham and Women's Hospital, Inc.
United States
The Senior Research Programmer/Analyst will support this mission as part of a highly collaborative multidisciplinary research environment comprising approximately 30 Harvard Medical School…
Added 17 days ago
NL
Senior Bioinformatics Programmer
NYU Langone Medical Center
New York, NY
- $90,000 to $115,000 USD / year
The Petljak Lab is seeking a highly motivated and creative Senior Bioinformatics Programmer to join our multidisciplinary team within the newly established Cancer Genomics & Genetics…
Added 18 days ago
Principal Statistical Programmer
IQVIA
Durham, NC
We are seeking a Principal Statistical Programmer to provide full end‑to‑end statistical programming support across clinical development programs. This role requires deep technical…
Added 21 days ago
Principal Statistical Programmer
BD (Becton, Dickinson and Company)
Irvine, CA
Provide hands‑on statistical programming support for clinical studies, including development and validation of analysis datasets and statistical outputs, in accordance with regulatory and…
Added 21 days ago
Biostatistical Analyst II (Remote Capable)
Geisinger
Danville, PA
Independently provides statistical consultations or collaborations with clinical principal investigators.
Added 21 days ago
Biostatistician
Geisinger
Danville, PA
Independently provides statistical consultations or collaborations with clinical principal investigators.
Added 22 days ago
Senior Programming Lead, Oncology
J&J Family of Companies
Raritan, NJ
Purpose: The Senior Programming Lead is an experienced programmer with an advanced knowledge of programming languages, has expertise in industry standards, complex data structures and…
Added 22 days ago
SAS Programmer Analysts
Munidex Inc
Piscataway, NJ
SAS Programmer Analysts (Piscataway, NJ) – Analyze and interpret data to develop business solutions using Generalized Linear Models, Logistic Regression Model; Program SAS software for…
Added 22 days ago
Senior Health Economics & Outcomes Research Analyst
Medtronic
Mounds View, MN
Experience working with large databases including health care claims, administrative, or patient discharge data as a health service researcher, epidemiologist, data programmer or economist
Added 22 days ago
Principal Medical Safety Specialist
Medtronic
Minneapolis, MN
As a Principal Medical Safety Specialist, Cardiac Rhythm Management, you will provide clinical and technical expertise to support patient safety activities across Cardiac Implantable…
Added 22 days ago
UO
Senior Data Analyst (5469C), California Policy Lab #88224
University of California, Berkeley
CA
- $95,000 to $130,000 USD / year
The Senior Data Analyst is an expert programmer who is fluent in multiple programming languages, has experience with SQL databases and large administrative datasets, and believes in CPL’s…
Added 22 days ago
Programmer
Harvard University
Boston, MA
We are seeking a Programmer to join our dynamic team. Duties and responsibilities include, but are not limited to, the following:
Added 23 days ago
Remote Principal Statistical Programmer
Global Channel Management, Inc
Cambridge, MA
Remote Principal Statistical Programmer needs 10 years Pharmaceutical/Biotech programming experience including macro/tools development experience.
Added 24 days ago
UU
Research Data Scientist
USC University of Southern California
Los Angeles, CA
- $105,664.88 to $122,141.8 USD / year
The Leonard D. Schaeffer Center for Health Policy & Economics is seeking a Research Data Scientist (HR title: Research Programmer II) to support cutting-edge health policy and economics…

BD (Becton, Dickinson and Company)

Principal Statistical Programmer

Irvine, CA, United States

$129,600 to $207,400 USD / year

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Job details

Pay: $129,600 to $207,400 USD / year
Experience: Master’s degree (or equivalent) in a related STEM field with 3+ years of relevant statistical programming experience
Posting language: English
Posted: Jul 29, 2026

Original job description

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us - from design and engineering to the manufacturing and marketing of our billions of MedTech products per year - to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

Role Purpose

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 standards. The Principal Statistical Programmer is expected to work independently, deliver high‑quality programming deliverables, and collaborate effectively with Biostatistics and Clinical Data Management.

Key Responsibilities

Primary Responsibilities

Develop complex analysis datasets, specifications, and summary outputs (tables, listings, figures, and graphs) for inclusion in clinical study reports, regulatory submissions, and internal presentations.
Create, modify, and maintain SAS programs that meet regulatory and company standards to ensure efficient programming, reporting, review, and traceability.
Perform independent program review and validation, ensuring complete, accurate, and inspection‑ready documentation in compliance with applicable regulations and internal procedures.
Support ad hoc and planned analyses in collaboration with the designated statistician, including responses to data review questions.
Partner with Clinical Data Management and Biostatistics to review CRFs, database specifications, edit checks, and data derivations as needed.
Proactively identify programming risks, data issues, or efficiency opportunities and communicate them clearly to study team members.

Scope & Level of Independence

Works independently with minimal supervision, receiving high‑level objectives and delivering agreed‑upon outputs.
Evaluates alternative programming approaches and applies sound judgment in accordance with regulatory and quality standards.
May provide technical guidance or support to other programmers, as appropriate.
Responsible for managing assigned programming tasks and timelines.

Required Skills/Experience:

Bachelor’s degree in Statistics, Mathematics, Computer Science, or a related field or other STEM Field with 5+ years of relevant statistical programming experienceOR
Master’s degree (or equivalent) in a related STEM field with 3+ years of relevant statistical programming experience
Demonstrated experience performing statistical programming in a clinical trials environment (pharmaceutical and/or medical device).
Strong hands‑on experience with SAS programming for clinical trial data including SAS Base, SAS/STAT, and SAS Macros.
Proven experience developing and validating:
Analysis datasets
Tables, listings, and figures
Solid understanding of regulatory requirements and guidelines applicable to clinical research (e.g., GCP, ICH, FDA, ISO).
Experience with CDISC standards (e.g., SDTM, ADaM).
Experience supporting programming deliverables that are inspection‑ready.
Proficiency interfacing SAS outputs with common productivity tools (e.g., Microsoft Excel, Word, PowerPoint).
Strong analytical, problem‑solving, and organizational skills.
High attention to detail and commitment to data quality.
Clear written and verbal communication skills.
Ability to collaborate effectively with cross‑functional stakeholders, including statisticians and data managers.
Ability to manage competing priorities in a fast‑paced project environment.

Preferred Skills/Experience

Prior participation in regulatory submissions or submissions‑related deliverables.
Experience reviewing or validating programming deliverables from CROs or vendors.
Development of SAS macros or tools that improve programming efficiency.
Ability to program in other statistical languages such as R or Python.

Additional Information

This role is an individual contributor position and does not include formal people‑management responsibilities.
The programmer is expected to adhere to all applicable quality, compliance, and safety requirements relevant to their work.

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers .

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Required Skills

Optional Skills

Primary Work Location

USA CA - Irvine Laguna Canyon

Additional Locations

Work Shift

NA (United States of America)

At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You (https://jobs.bd.com/en/your-career-at-BD) ."

Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.

Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.

Salary Range Information

$129,600.00 - $207,400.00 USD Annual

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

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More about this job

Skills

Work independently
Data management
SAS
Reporting
Inspection
Documentation
Regulatory compliance
Collaboration
Statistics
Computer science
Clinical trials
SAS/STAT
Clinical research
Google Cloud
Microsoft Excel
Microsoft Word
Microsoft PowerPoint
Problem solving
Organizational skills
Attention to detail
Communication skills
R
Python

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