Principal Statistical Programmer

Becton Dickinson; United States; On-site; USD 120,000 - 165,000; Full time

Job summary

Becton Dickinson seeks an experienced Principal Statistical Programmer to provide hands-on SAS programming support for clinical studies. You will develop analysis datasets and create tables, listings, and figures for reports and submissions, while ensuring regulatory and company standards.

The role requires independent work, collaboration with Biostatistics and CDM, and a proactive approach to risk and data quality in a fast-paced environment. On-site presence is expected at most sites.

Qualifications

• Bachelor's degree with 5+ years in statistical programming in clinical trials or medical devices.
• Master's degree with 3+ years in statistical programming in relevant settings.

Responsibilities

• Develop and maintain complex SAS programs for analysis datasets, tables, listings, and figures for reports and submissions.
• Perform independent program review and validation with complete documentation per regulatory standards.
• Support ad hoc analyses and responses to data review questions in collaboration with statisticians and data management.
• Partner with Clinical Data Management and Biostatistics to review CRFs, database specs, and data derivations.
• Identify programming risks and data issues, communicating findings clearly to study teams.

Skills

SAS programming

SDTM/ADaM

Clinical trials

Regulatory compliance

Data management

Cross-functional collaboration

Attention to detail

Statistical analysis

Education

Bachelor's degree in Statistics, Mathematics, Computer Science, or related field

Master's degree in related STEM field

Tools

SAS Base

SAS/STAT

SAS Macros

CDISC SDTM

CDISC ADaM

Excel

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 experience
• OR
• 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 COV