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Manager Statistical Programming Jobs in Baltimore, MD

Amgen

Biostatistical Prograrmming Manager

Baltimore, MD · On-site

In this vital role you will provide both strategic oversight and hands-on statistical programming ... The manager will serve as a technical programming expert who can rapidly respond to internal and ...

Axle

Computer Systems Analyst

Baltimore, MD

With experts in biomedical science, software engineering, and program management, we focus on ... Provide statistical support to staff, including data analysis and the generation tools for ...

Axle

Computer Systems Analyst

Baltimore, MD · On-site

With experts in biomedical science, software engineering, and program management, we focus on ... Provide statistical support to staff, including data analysis and the generation tools for ...

Deloitte

AWS Sales Engineer

Baltimore, MD · On-site

... statistical programming tools to enterprise data in order to advance and enable the key mission ... Strong project management and organizational skills, with the ability to manage multiple priorities ...

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All JobsManager Statistical Programming JobsManager Statistical Programming Jobs in Baltimore, MD

Manager Statistical Programming information

See Baltimore, MD salary details

$84K

$146.4K

$247.4K

How much do manager statistical programming jobs pay per year?

As of Jun 27, 2026, the average yearly pay for manager statistical programming in Baltimore, MD is $146,355.00, according to ZipRecruiter salary data. Most workers in this role earn between $124,200.00 and $159,000.00 per year, depending on experience, location, and employer.

What is a Manager Statistical Programming job?

A Manager Statistical Programming oversees a team of statistical programmers who support clinical trials and research by developing, validating, and maintaining statistical programs. They ensure compliance with regulatory requirements, manage project timelines, and collaborate with statisticians, data managers, and other stakeholders. This role requires strong programming skills in SAS or other statistical software, leadership abilities, and expertise in clinical data standards such as CDISC.

What are the typical daily responsibilities of a Manager Statistical Programming?

As a Manager Statistical Programming, your daily responsibilities usually include overseeing a team of statistical programmers, coordinating the development and validation of statistical programs for clinical trial data analysis, and ensuring deliverables meet regulatory and company quality standards. You will often interact with biostatisticians, data managers, and clinical teams to align programming outputs with study goals. Additionally, you may review project timelines, allocate resources, mentor junior programmers, and contribute to process improvement initiatives. This multifaceted role requires balancing technical oversight with leadership and interdepartmental communication.

What are the key skills and qualifications needed to thrive in the Manager Statistical Programming position, and why are they important?

To excel as a Manager Statistical Programming, you need a solid background in statistics, programming (such as SAS, R, or Python), and experience with clinical trial data management, often supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory guidelines (e.g., FDA, ICH), data standards such as CDISC, and certifications in relevant programming languages or clinical data processes are highly beneficial. Strong leadership, project management, and effective communication skills are essential for guiding teams and collaborating with cross-functional departments. These skills enable the manager to deliver high-quality statistical programming deliverables, ensure regulatory compliance, and drive team performance in a deadline-driven environment.

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What cities near Baltimore, MD are hiring for Manager Statistical Programming jobs? Cities near Baltimore, MD with the most Manager Statistical Programming job openings:
Manager Statistical Programming jobs near you

Sr. Statistical Programmer

Katalyst Healthcares and Life Sciences

Baltimore, MD • On-site

Other

Posted 4 days ago

Job description

Job Description:
  • We are seeking a highly motivated and qualified individual to join our Clinical Department as a SeniorStatistical Programmer and work as part of a team to drive success.
  • Ideal candidates will be self-motivated, independent, committed to the generation of high-quality data within a fast-paced and innovative research team.
  • The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings, summary tables, and statistical graphs supporting statistical analyses.
  • This position requires close collaboration with cross-functional teams to ensure the integrity and accuracy of clinical data used in regulatory filings and internal reporting.

Responsibilities:
  • Independently develop, validate, document and troubleshoot SAS programs for the preparation of periodic internal reports, regulatory submissions, and ad hoc analyses.
  • Create and maintain analysis and submission datasets (ADaM, SDTM) in compliance with CDISC standards and regulatory guidance.
  • Design, develop, validate, update, and document SAS programs to generate analysis datasets, data listings, tables, and graphs of high quality in a timely manner.
  • Support submission activities including preparation of data packages, eCTD deliverables, and responses to regulatory agencies,
  • Communicate with team members about statistical programming related to trial timelines, data quality, and results interpretation.
  • Develop software tools, SAS macros and utilities to automate programming activities and improve programming efficiency and quality.
  • Create SAS macros or other tools to enhance the efficient delivery of statistical services, providing associated documentation and staff training as needed.
  • Program quality checks for clinical study raw data and report findings.
  • Review or author SDTM and ADaM specifications and datasets.
  • Manage CROs, including reviewing or validating statistical deliverables of vendors.
  • Provides input in the design and development of case report forms.
  • Contribute to the preparation of research reports and presentations for internal project teams, leadership team, and external audience.
  • Establish and maintain excellent working relationships with critical collaborative partners throughout the company.
Requirements:
  • Bachelor's degree in Biostatistics, Mathematics, Statistics, Computer Science, or related field
  • Minimum 6 years' experience in bio-pharma statistical programming
  • dvanced SAS programming skills in SAS/Base, SAS/Macro, SAS/STAT, SAS/Graph, and SAS/SQL with a demonstrated mastery of SAS/STAT procedures
  • Strong expertise in CDISC including SDTM, ADaM, and CDASH
  • Extensive experience in SAS macro functions and dynamic code generations.
  • Experience in regulatory submissions (e.g., NDAs and DSURs)
  • High attention to detail, with a focus on quality and traceability in all deliverables
  • Strong interpersonal and teamwork skills with a collaborative mindset and the ability to manage multiple priorities in a fast-paced and dynamic environment with shifting timelines and evolving needs
  • Take initiatives to solve problems proactively and think critically
  • Willing to adapt to changing business needs, able to pivot between tasks
  • ble to make complex programming and data-related decisions independently
  • Comprehensive knowledge and deep understanding of statistical programming environments, processes, procedures, and roles for clinical development from Phase 1 through regulatory submission
  • Up to date with CDISC standards, industry trends, best practices, and statistical programming methodology

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