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Associate Statistical Programmer Jobs in Philadelphia, PA

Bread Financial

Lead Data Scientist

Chadds Ford, PA · On-site +1

$144K - $250K/yr

Bachelor's Degree in Statistics, Mathematics, Engineering, Data Science, Computer Science, or ... New associate elected coverage begins on date of hire (with the exception of disability coverage ...

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All JobsAssociate Statistical Programmer JobsAssociate Statistical Programmer Jobs in Philadelphia, PA

Associate Statistical Programmer information

See Philadelphia, PA salary details

$85.3K

$148.6K

$251.3K

How much do associate statistical programmer jobs pay per year?

As of Sep 3, 2026, the average yearly pay for associate statistical programmer in Philadelphia, PA is $148,630.00, according to ZipRecruiter salary data. Most workers in this role earn between $126,100.00 and $161,500.00 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 Philadelphia, PA?

The most popular types of Statistical Programmer jobs in Philadelphia, PA are:

What are popular job titles related to Associate Statistical Programmer jobs in Philadelphia, PA?

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

What job categories do people searching Associate Statistical Programmer jobs in Philadelphia, PA look for?

The top searched job categories for Associate Statistical Programmer jobs in Philadelphia, PA are:

Associate Statistical Programmer jobs near you
Infographic showing various Associate Statistical Programmer job openings in Philadelphia, PA as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 26% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $148,630 per year, or $71.5 per hour.

(Associate) Scientist, Upstream Viral Process Development

Dispatch Bio

Philadelphia, PA

Full-time

Re-posted 14 days ago

Job description

The role:

Reporting to the Director, Upstream Process Development, the (Associate) Scientist will contribute to upstream viral process development to bring the company's pipeline of T cell and viral vector-based products to the clinic. Responsibilities will include, but are not limited to, performing the day-to-day activities of the viral process development lab, building the company's viral manufacturing capabilities, and executing experiments to support viral process development/characterization. This role will collaborate significantly with research and analytical development teams. 

Key responsibilities:

  • Contribute to the setup and organization of the company's vector process development capabilities. 
  • Perform day-to-day activities in the vector process development lab including maintaining equipment, ordering materials, managing inventory, and preparing buffers and process aids. 
  • Serve as a PD subject matter expert on both internal and external teams (CDMO, material & equipment suppliers, etc.). 
  • Develop bench scale suspension culture processes for viral vector generation within shake flasks and bioreactors. 
  • Design and execute experiments to support process characterization, and process transfer activities between the research team, TechOps, and external partners. 
  • Provide experimental execution, data review and analysis, and maintenance of accurate and detailed lab notebooks. 
  • Author and review technical documents, including but not limited to batch records, SOPs, development reports and process specific sections of regulatory documents. 
  • Represent the company externally at meetings (professional associations, with regulatory bodies, etc.) 

Required experience & skills:

  • Bachelor's Degree in chemical engineering, biochemical engineering/bioengineering, biotechnology or related discipline with at least 2 years of relevant experience- OR- Master's Degree in relevant discipline 
  • Hands-on experience with viral vector upstream processes, particularly experimentation in and operation of stirred-tank bioreactors 
  • Working knowledge of GMP guidelines for clinical manufacturing 
  • Strong scientific reasoning, problem-solving, and applied mathematics and statistics skills, including the ability to break down complex problems into manageable hypotheses 
  • Proficiency in using Microsoft Word, Excel, Power Point and data analysis/presentation software such as JMP and/or GraphPad 
  • Excellent interpersonal, verbal and written communication skills 
  • Strong organizational & problem-solving skills, with excellent attention-to-detail and the proven ability to collaborate in a dynamic team environment 

Preferred experience & skills:

  • Experience implementing processes in clinical and commercial manufacturing of cell and gene therapy products 
  • Demonstrated ability to apply knowledge of cell biology, chemical engineering, or bioengineering toward process development, scale-up /scale-down and troubleshooting 
  • Detailed understanding of bioreactor operation and control loops 
  • Experience drafting CMC sections for INDs 
  • Proven experience collaborating with internal and external partners 

 

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