Top 11 Sas programmer Jobs in Maryland

SAS Programmer
PMTS, Inc —Frederick, MD
- $95,000 - $120,500 a year
- Full-time
- Computer Science
- Mid-level
- Office
- Health insurance
- Dental insurance
Quick Apply
SAS Programmer
CICONIX, LLC —Fort Detrick, MD
- Full-time
- Background check
- Mid-level
- Office
- Paid time off
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Senior Statistical Programmer
TEKaroon —Elkridge, MD
- Email
- Computer Science
- Analysis skills
- Mentoring
Research Data Analyst/Programmer (Open Rank: Senior, Lead, Manager)
University of Maryland, Baltimore —Baltimore, MD
- $65,070 - $104,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- System design
- Office
- Paid holidays
- Disability insurance
8d
Developer (Bayview Pediatrics)
Johns Hopkins University —Baltimore, MD
- $50,440 - $88,400 a year
- Full-time
- Background check
- Mid-level
- University
Sr. Statistical Programmer
Katalyst Healthcares & Life Sciences —Baltimore, MD
- Contract
- Computer science
- 6 years
- Computer Science
Quick Apply
Manager, Statistical Programming
Supernus Pharmaceuticals Inc —Rockville, MD
- $100,000 - $130,000 a year
- Computer Science
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
Senior Manager, Clinical Data Standards
Immunocore —Gaithersburg, MD
- $121,500 - $202,500 a year
- Full-time
- Computer Science
- Master's degree
- SQL
Computer Systems Analyst
Axle —Baltimore, MD
- $115,000 - $125,000 a year
- Computer Science
- Mid-level
- Team management
- Paid holidays
- Health insurance
Quick Apply
Computer Systems Analyst
GAP SOLUTIONS INC —Baltimore, MD
- $140,000 - $160,000 a year
- Email
- Computer Science
- 11+ years
- Mid-level
Quick Apply
Senior Manager, Analytics Engineering
GEICO —Bethesda, MD
- $130,000 - $260,000 a year
- Full-time
- Azure
- Windows
- SQL

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SAS Programmer
PMTS, Inc —Frederick, MD
The selected candidate will develop and validate SAS programs that produce CDISC-compliant clinical trial datasets, statistical tables, listings, and figures (…
$95,000 - $120,500 a year
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Research Assistant/Associate - Junior Evaluator
MayaTech Corporation —Silver Spring, MD
The MayaTech Corporation seeks Evaluation staff to assist in the support of national research projects and grantee efforts and collaborate in the design,…

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Mainframe Systems Engineer III
Huntington Bank —Columbus, OH
Mentors and assists Infrastructure resources on infrastructure service along with application integration validation methods and tools to ensure that technology…
$70,000 - $140,000 a year

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SAS Programmer

PMTS, Inc
Frederick, MD

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Job Details

Full-time
$95,000 - $120,500 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Life insurance

Qualifications

Statistics
Statistics
SAS
Technical documentation
SAS language
SQL
ICH guidelines
Technical writing experience within healthcare
Bachelor's degree
CDISC standards
Biomedical regulatory compliance
Clinical quality assurance standards
Project stakeholder communication
Python
Data analysis software
Database software proficiency

Full Job Description

Job Overview
Program Management and Technology Services, Inc. (PMTS) is seeking a SAS Programmer to support the Defense Health Agency (DHA) Research and Development MRDC Office of Regulated Activities (ORA) at Fort Detrick, MD. This is a contingent position pending award of a federal GSA MAS task order with a target start date of August 1, 2026.

The SAS Programmer is a Designated Key Personnel role providing clinical statistical programming and data analytics support across a portfolio of FDA-regulated medical product development programs. The selected candidate will develop and validate SAS programs that produce CDISC-compliant clinical trial datasets, statistical tables, listings, and figures (TLFs) in support of regulatory submissions including INDs, NDAs, BLAs, 510(k)s, PMAs, and integrated summaries. This role works closely with the Senior Biostatistician, Clinical Database Developer, and Medical Writers to deliver high-quality, submission-ready statistical work products.

Responsibilities

Develop, test, validate, and document SAS programs supporting clinical trial analysis, regulatory submissions, and ad hoc statistical reporting per the Statistical Analysis Plan
Produce CDISC SDTM and ADaM analysis datasets and define.xml metadata in accordance with current FDA and CDER Technical Conformance Guide requirements
Generate publication-quality Tables, Listings, and Figures (TLFs) for Clinical Study Reports, Integrated Summaries of Safety (ISS), Integrated Summaries of Efficacy (ISE), and other regulatory deliverables
Perform independent programmatic validation (double programming) of statistical outputs and resolve discrepancies in collaboration with lead statisticians
Develop and execute edit checks, data reconciliation programs, and quality-control routines on clinical trial data, supporting database lock readiness
Support pharmacokinetic, pharmacodynamic, and exposure-response analyses, including production of PK/PD datasets and supporting deliverables
Collaborate with the Senior Biostatistician on Statistical Analysis Plan development, sample size calculations, and analytical methodology
Maintain comprehensive program documentation, version control, and audit trails compliant with 21 CFR Part 11 and applicable ORA standards
Participate in protocol review, CRF design review, and Data Management Plan development to ensure downstream analyzability of clinical trial data
Support FDA submission and review activities including responses to FDA information requests and preparation of submission datasets in eCTD-ready format

Required Qualifications

Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, Epidemiology, or a related quantitative field; Master's degree preferred
Minimum 4 years of professional clinical SAS programming experience in pharmaceutical, biotechnology, medical device, CRO, or government clinical research settings
Demonstrated expertise in Base SAS, SAS/STAT, SAS/GRAPH, SAS Macro Language, and SQL; proficiency in CDISC SDTM and ADaM standards
Hands-on experience producing TLFs and analysis datasets for at least one regulatory submission (IND, NDA, BLA, 510(k), PMA, or equivalent)
Working knowledge of ICH E9, FDA Statistical Software Guidance, and 21 CFR Part 11 compliance requirements for electronic records
Strong written and verbal communication skills; ability to document programming logic and communicate statistical concepts to non-statistical stakeholders
U.S. citizenship required; ability to obtain and maintain a T1/HSPD-12 Public Trust investigation

Preferred Qualifications

Master's degree (MS, MPH, or equivalent) in Biostatistics, Epidemiology, or Statistics
CDISC SDTM and/or ADaM Advanced certification
Experience supporting DoD, NIH, BARDA, or other federal clinical research programs (USAMRDC, WRAIR, Fort Detrick, NCI, or NIAID preferred)
Working knowledge of R, Python, or other complementary statistical programming environments
Experience with SEND (Standard for Exchange of Nonclinical Data) for FDA toxicology submissions
Familiarity with statistical computing environments used in federal research settings (SAS Grid, SAS Viya, or AWS-hosted SAS environments)
Experience supporting multi-protocol programs, oncology, vaccines, or medical countermeasures

Pay: $95,000.00 - $120,500.00 per year

Benefits:

401(k)
Dental insurance
Health insurance
Life insurance
Paid time off
Vision insurance

Work Location: In person

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sas programmer jobs in maryland

SAS Programmer

SAS Programmer

Senior Statistical Programmer

Research Data Analyst/Programmer (Open Rank: Senior, Lead, Manager)

Developer (Bayview Pediatrics)

Sr. Statistical Programmer

Manager, Statistical Programming

Senior Manager, Clinical Data Standards

Computer Systems Analyst

Computer Systems Analyst

Senior Manager, Analytics Engineering

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