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Associate Statistical Programmer Jobs in Maryland

Spruce Infotech

SAS Programmer Analyst

Baltimore, MD · On-site

$90 - $120/hr

Associate's degree with 16 years of relevant experience Desired Qualifications * Experience with ... Experience with statistical modelling tools. * Experience with Data Presentation/Visualization ...

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All JobsAssociate Statistical Programmer JobsAssociate Statistical Programmer Jobs in Maryland

Associate Statistical Programmer information

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$143K

$241.7K

How much do associate statistical programmer jobs pay per year?

As of Aug 27, 2026, the average yearly pay for associate statistical programmer in Maryland is $142,952.00, according to ZipRecruiter salary data. Most workers in this role earn between $121,300.00 and $155,300.00 per year, depending on experience, location, and employer.

What is an associate statistical programmer?

An Associate Statistical Programmer is an entry-level professional who assists in the programming and analysis of clinical trial data, primarily within the pharmaceutical or biotechnology industries. They use statistical software, such as SAS or R, to create, validate, and maintain datasets, tables, listings, and figures required for clinical study reports. Their work supports biostatisticians and clinical teams in ensuring data accuracy and regulatory compliance. This role is ideal for those with a background in statistics, mathematics, or computer science, looking to start a career in clinical data analysis.

How does an associate statistical programmer typically collaborate with biostatisticians and data managers in clinical research projects?

As an Associate Statistical Programmer, you will frequently collaborate with biostatisticians to understand statistical analysis plans and translate them into clear programming specifications. You’ll also work closely with data managers to ensure data integrity and resolve any data discrepancies before analysis. Effective communication and teamwork are essential, as you’ll often participate in project meetings, provide programming support, and help deliver high-quality datasets and reports under tight timelines. This collaborative environment is key to ensuring accurate and timely clinical trial results.

What are the key skills and qualifications needed to thrive as an associate statistical programmer, and why are they important?

To thrive as an Associate Statistical Programmer, you need a solid background in statistics, programming (especially SAS or R), and familiarity with clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Proficiency with statistical software (such as SAS, R, or Python), CDISC standards, and data management tools is essential, and certifications in SAS programming can be advantageous. Attention to detail, strong problem-solving abilities, and effective communication skills help you collaborate with clinical teams and ensure data quality. These skills and qualities are vital for delivering accurate statistical analyses that support regulatory submissions and evidence-based decision-making in clinical research.

What is the difference between Associate Statistical Programmer vs Statistical Programmer?

AspectAssociate Statistical ProgrammerStatistical Programmer
Required CredentialsBachelor's degree in statistics, mathematics, or related field; some roles may require basic programming skillsBachelor's or master's degree; more experience in programming and statistical analysis
Work EnvironmentEntry-level, supporting senior programmers; often in clinical research or pharmaceutical companiesMore independent, handling complex analyses; similar industry settings
Employer & Industry UsageCommon in clinical trials, pharmaceutical, and biotech companiesUsed across similar industries, often as a step up from associate roles

The main difference between an Associate Statistical Programmer and a Statistical Programmer lies in experience and responsibility level. Associate roles are typically entry-level, focusing on supporting tasks under supervision, while Statistical Programmers handle more complex analyses independently. Both roles are vital in clinical research and biotech industries, with the associate position serving as a stepping stone to more advanced programming roles.

What are the most commonly searched types of Statistical Programmer jobs in Maryland?

The most popular types of Statistical Programmer jobs in Maryland are:

What are popular job titles related to Associate Statistical Programmer jobs in Maryland?

For Associate Statistical Programmer jobs in Maryland, the most frequently searched job titles are:

What job categories do people searching Associate Statistical Programmer jobs in Maryland look for?

The top searched job categories for Associate Statistical Programmer jobs in Maryland are:

Associate Statistical Programmer jobs near you
Infographic showing various Associate Statistical Programmer job openings in Maryland as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 24% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $142,952 per year, or $68.7 per hour.

Senior Specialist Programmer

Fladger Associates

Gaithersburg, MD • On-site

Contractor

Re-posted 17 days ago

Job description

Gaithersburg, MD
Contract Duration: 12-36 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a Senior Specialist Programmer in the Gaithersburg, MD area. (100% remote)
  • The Senior Statistical Programmer is a delivery focused role responsible for programming deliverables with quality and timeliness, following established standards and processes.
  • This position requires high technical skills and thorough industry knowledge to independently perform the programming tasks while using judgement about seeking guidance in complex situations.
  • They can be responsible for leading the programming deliveries of clinical studies or small to medium sized clinical projects and can lead cross-functional teams to deliver continuous improvement
  • Primarily responsible for coordinating the various tools for collecting different types of data.
  • Responsible for ensuring databases are created and adjusted for the end user.
  • Contributes to the development and maintenance of analysis and reporting applications.
  • Able to solve complex problems within own area and will participate in a range of projects.
  • Responsible for leading the programming deliveries of a clinical study or a small to medium sized and complex clinical project
  • Implements statistical programming aspects of the protocol or clinical development program
  • Ensures high quality is built into own deliverables and the quality delivered by other programmers
  • Programs independently with high efficiency and quality
  • Writes specifications and oversee completeness of relevant documentation
  • Contributes to or drives the development of best practices to improve quality, efficiency and effectiveness within function
  • Ensures compliance to standards and automation usage
  • Plans and leads team activities and tasks
  • Identifies, manages and communicates risk within the assigned studies and/or projects
  • Works proactively with study team members including but not limited to the statistician, lead programmer, data manager and study leader
  • Works cooperatively with contract programming providers
  • Influences stakeholders by providing subject matter expertise on programming related items
  • Contributes to or leads technical initiatives
  • Employs Project Management practices in managing programming aspects of drug or technical projects
Experience:
  • Vaccine experience highly desired
  • Bachelor's Degree in Mathematics (i.e., Applied Math, Engineering, etc.), Statistics, Computer Science, Life Science or equivalent
  • 8-10 years of strong Programming experience
    Ability to proactively manage concurrent activities within a study or part of project
  • Excellent programming skills including macro language
  • Proficient knowledge of the clinical development process
  • Thorough knowledge of industry standards
  • Ability to apply Programming knowledge to problem solving
  • Ability to manage relevant documentation
  • Ability to influence relevant stakeholders on Programming related items
  • Ideally candidate would have previous vaccine experience.
  • Ability to proactively manage concurrent activities within a study or part of project