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Statistical Programmer Jobs in Philadelphia, PA (NOW HIRING)

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... statistical programming languages/software such as SAS and/or R · Able to work in a virtual environment · Teamwork and leadership skills · Technical expertise and application with working ...

R&D Programmer II

West Chester, PA · On-site

$61 - $73/hr

Clinical Programming - Contractor - Analysis and Reporting (ADaM) Remote Duration: Up to 2 year ... Bachelor's Degree/Master's Degree in Science, Statistics, Information Technology or equivalent ...

This role is ideal for a candidate who combines traditional clinical statistical programming expertise with hands-on application development, data pipeline automation, and standards-driven clinical ...

Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing Management & Operations etc. Who is proficient in Customer-level data analysis. Qualifications Who ...

Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing Management & Operations etc. Who is proficient in Customer-level data analysis. Qualifications Who ...

Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing Management & Operations etc. Who is proficient in Customer-level data analysis. Qualifications Who ...

Act as the primary programming point of contact for biostatisticians and study teams 5.Perform peer ... Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO. 3.In-depth knowledge of CDISC standards and ...

Provide statistical consultancy support to sponsors across the full span of clinical development, including oversight of third-party statistical and programming deliverables. * Maintain current ...

Showing results 41-60

Statistical Programmer information

See Philadelphia, PA salary details

$85.3K

$148.6K

$251.3K

How much do statistical programmer jobs pay per year?

As of Sep 6, 2026, the average yearly pay for 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 a statistical programmer?

Statistical programmers are professionals who use statistical software and programming languages, such as SAS, R, or Python, to manage, analyze, and report data, often in clinical trials, public health, or research settings. They play a crucial role in transforming raw data into meaningful results by writing code for data cleaning, data manipulation, statistical analysis, and generating reports. Statistical programmers often work closely with statisticians, data managers, and researchers to ensure the accuracy and integrity of data analyses. Their work is essential in industries like pharmaceuticals, healthcare, and academia.

What does a statistical programmer do?

A statistical programmer creates statistical programming deliverables. You ensure excellent programming of analysis-ready data, tables, and figures. You may use Stata for general purpose statistical analysis or SPSS for interactive or batched statistical analysis. Your responsibilities include developing standard operating procedures and complying with guidelines. Other duties include remaining informed on developments in programming standards and meeting all regulatory requirements. You also create PROC statements that call upon named procedures for analysis. You develop programs for dataset integration, prepare resource plans, and assist with quality control of datasets.

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

To thrive as a Statistical Programmer, you need a strong background in statistics, data analysis, and programming—typically with a degree in statistics, mathematics, computer science, or a related field. Expertise in statistical software such as SAS, R, or Python and familiarity with data management systems like CDISC or SQL are often required, along with relevant certifications. Strong problem-solving abilities, attention to detail, and clear communication skills help you interpret data accurately and collaborate effectively with cross-functional teams. These skills ensure the delivery of high-quality, reproducible statistical analyses crucial for informed decision-making in research and industry settings.

What are some common challenges faced by statistical programmers when working on clinical trial data?

Statistical Programmers often encounter challenges such as managing large, complex datasets, ensuring data integrity, and adhering strictly to regulatory standards (like CDISC SDTM and ADaM). They must also collaborate closely with biostatisticians and data managers to accurately translate statistical analysis plans into code. Tight project timelines and shifting priorities can require strong organizational skills and adaptability. Effective communication and attention to detail are essential for navigating these challenges and delivering reliable results.

What is the difference between Statistical Programmer vs Data Analyst?

AspectStatistical ProgrammerData Analyst
Required CredentialsBachelor's in Statistics, Biostatistics, or related field; experience with SAS, R, or PythonBachelor's in Statistics, Data Science, or related field; proficiency in Excel, SQL, and visualization tools
Work EnvironmentPharmaceutical, clinical research, or healthcare industries; focus on programming and data managementVarious industries including finance, marketing, healthcare; focus on data interpretation and reporting
Employer & Industry UsageCommon in clinical trials, biotech, pharma companiesUsed across multiple sectors like finance, retail, and healthcare

While both roles handle data, Statistical Programmers primarily focus on programming and managing clinical or research data, whereas Data Analysts interpret data to generate insights across various industries. The roles often overlap in skills like statistical software proficiency but differ in their core responsibilities and industry focus.

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 Statistical Programmer jobs in Philadelphia, PA?

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

What cities near Philadelphia, PA are hiring for Statistical Programmer jobs?

Cities near Philadelphia, PA with the most Statistical Programmer job openings:

Infographic showing various Statistical Programmer job openings in Philadelphia, PA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Remote job distribution, with an average salary of $148,630 per year, or $71.5 per hour.

Senior Scientist, Biostatistics, Clinical Safety Statistics

MSD Malaysia

North Wales, PA • On-site

$117 - $184/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago


Key responsibilities

  • Provide statistical support for program-level evaluation of clinical safety data.

  • Plan, execute, and evaluate ongoing aggregate safety evaluations, including cumulative meta-analyses of safety.

  • Design, develop, and apply safety evaluation methods, processes, standards, and tools, including graphical analyses.


Job description

Job Description BARDS (Biostatistics and Research Decision Sciences)

BARDS (Biostatistics and Research Decision Sciences) is a distinguished department within our company's renowned Research and Development division. Quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health.

The Clinical Safety Statistics (CSS) group within BARDS supports proactive assessment, transparent communication, and effective management of product risk profiles in pre- and post-marketing development stages.

Responsibilities: Provide statistical support for program-level evaluation of clinical safety data. Interact with members of cross-functional safety teams (e.g., Safety Physicians and Scientists, Clinical Trial Physicians and Scientists, Epidemiologists, Regulatory Liaisons, Early and Late Development Statisticians, Statistical Programmers, and others) on the planning and execution of ongoing safety evaluations for products across pre-marketing and post-marketing development stages. Design, develop and evaluate processes and tools for product safety evaluation, including ongoing aggregate safety evaluation at the program level.

Primary activities
  • Provide statistical support to cross-functional safety teams including strategic planning and scientific reasoning activities that facilitate safety evaluation.
  • Plan and execute ongoing aggregate safety evaluations, including cumulative meta-analysis of safety.
  • Design, develop and apply safety evaluation methods, processes, standards, and tools, including enhanced graphical analyses.
  • Collaborate with other statisticians and statistical programming staff to ensure high-quality, safety-related deliverables, which meet analysis requirements, internal standard operating procedures, and external regulatory requirements.
  • Prepare oral or written reports to effectively communicate results of safety evaluations to project teams.
  • Ascertain the need for development of novel statistical methodology and evaluate the appropriateness of available software for implementing the planned analyses.
  • Conduct research on innovative statistical methods and applications in clinical safety evaluation.
Education and Minimum Requirement

PhD or equivalent degree in statistics/biostatistics or related discipline, or a master’s degree with a minimum of 3 years of relevant experience.

Required Skills and Experience
  • Solid understanding of study design and statistical analysis methods, particularly survival analysis, meta-analysis, and Bayesian methodologies.
  • Working knowledge of statistical and data processing software such as SAS and R (R-Shiny a plus).
  • Strong oral and written communication skills, with the ability to collaborate effectively with colleagues from different functional backgrounds.
  • Strong initiative, motivation, attention to detail, commitment to high-quality execution, and ability to manage multiple priorities.
Preferred Skills and Experience
  • Familiarity with CDISC standards, including SDTM and ADaM datasets.
  • Knowledge of statistical methods for analyzing observational epidemiologic data, including approaches to controlling confounding, such as matching and propensity score methods.
  • Proficiency in using AI tools to support writing activities (including summaries, reports, presentations, and manuscripts) as well as programming and other analytical tasks.
  • Knowledge of regulatory requirements related to safety signal detection, evaluation, and reporting.
  • Understanding of the drug discovery and development process.
  • Understanding of disease biology.
  • Interest in statistical research, particularly methodologies for safety monitoring, safety evaluation, and benefit-risk assessment; publication(s) in peer-reviewed statistical or medical journals a plus.
BARDS2020 #EligibleforERP Required Skills

Biostatistics, Clinical Trials, Data Management, Data Science, Scientific Modeling, Statistical Analysis, Statistics

Preferred Skills

US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.

If you need an accommodation during the application or hiring process.

Equal Employment Opportunity Statement

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.

As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.

For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts

Salary Range

The salary range for this role is $117,000.00 - $184,200.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting.

An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

Benefits
  • medical, dental, vision healthcare and other insurance benefits (for employee and family)
  • retirement benefits, including 401(k)
  • paid holidays
  • vacation
  • compassionate and sick days

More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

The application deadline for this position is stated on this posting.

San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status: Regular Relocation: Domestic VISA Sponsorship: Yes Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: Not Indicated Valid Driving License: No Hazardous Material(s): n/a Job Posting End Date: 09/7/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

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