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Senior Statistical Programmer Jobs in Philadelphia, PA

Ra

Marketing Analytics Senior Manager

Wilmington, DE · On-site

Senior Level This is what you will do.. You will be using quantitative methods to assess the impact ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

Ra

Marketing Analytics Senior Manager

Philadelphia, PA · On-site

Senior Level This is what you will do.. You will be using quantitative methods to assess the impact ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

Certara USA, Inc.

Senior SAS Developer

Wayne, PA · On-site

We are seeking a highly skilled Senior SAS developer to support Clinical Data Automation with ... This role is ideal for a candidate who combines traditional clinical statistical programming ...

Ra

Marketing Analytics Manager

Wilmington, DE · On-site

Mid - Senior Level This is what you will do.. You will be using quantitative methods to assess the ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

Ra

Marketing Analytics Manager

Philadelphia, PA

Mid - Senior Level This is what you will do.. You will be using quantitative methods to assess the ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

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Senior Statistical Programmer information

See Philadelphia, PA salary details

$83.3K

$129.5K

$169K

How much do senior statistical programmer jobs pay per year?

As of Sep 4, 2026, the average yearly pay for senior statistical programmer in Philadelphia, PA is $129,459.00, according to ZipRecruiter salary data. Most workers in this role earn between $108,000.00 and $149,300.00 per year, depending on experience, location, and employer.

What is a senior statistical programmer?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

What are the typical responsibilities and team dynamics for a senior statistical programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

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

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

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:

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

Senior Statistical Programmer jobs near you
Infographic showing various Senior Statistical Programmer job openings in Philadelphia, PA as of August 2026, with employment types broken down into 1% Internship, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $129,459 per year, or $62.2 per hour.

Principal Biostatistician

INC Research

King Of Prussia, PA

Full-time

Re-posted 20 days ago

Syneos Health rating

8.1

Company rating: 8.1 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

39th of 86 rated pharmaceutical

Job description

Company Description

INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world's pharmaceutical, biotech and medical device industries. We do this across six continents, and we'll do it for you too.

Job Description
    Provides biostatistics consulting in the design of protocols, drug development plans, and in the analysis and reporting of clinical trial data for all phases of drug development research.
    Assists in the development of policies, procedures and standards for biostatistics activities.  Supports the development and implementation of standard operating procedures and training program for staff.
    Participates in the sales and marketing function as it relates to operational activities.  Provides input and review/approval of study proposals upon request.
    Interacts with senior management of pharmaceutical and biotechnology sponsors on operational issues.
    Develops articles and presentations to be published in statistical journals and industry publications to promote the processes and technologies deployed by the biostatistics department.
    Ensures compliance with Good Clinical Practices, sponsor contracts as well as all Food and Drug Administration, and International Conference on Harmonization requirements.
    Maintains activity and visibility level providing representation for Company at professional meetings, including presentations at industry meetings, and other meetings relating to ICH issues or worldwide trends in biostatistics.
    Acts as mentor and technical expert to junior biostatisticians and programming staff.  Provides leadership, quality review, and mentoring to less experienced biostatisticians and coordinates the work of other biostatisticians.


Qualifications

    Requires a Ph.D. in Biostatistics, or in science with statistics minor or equivalent, plus moderate design and analysis of clinical trials experience in a Contract Research Organization or Pharmaceutical/ Biotechnology company OR an MS degree plus more experience, or equivalent in education and experience.  
    A nominal amount of supervisory experience preferred. 
    Requires in-depth knowledge and application of FDA/ICH regulations and experience in interacting with the FDA. 
    Expert knowledge of major statistical software program, e.g. SAS is necessary. 
    Strong working  knowledge of other software such as StatXact, Nonlin and EaSt is preferred. 
    Experience preparing and submitting regulatory documents is required. 
    Data management experience is preferred.
     Highly effective presentation, documentation, negotiation, interpersonal and leadership skills with a team-oriented approach are necessary. 
    Strong computer skills in Microsoft Office Suite are necessary. 
    The ability to prioritize and handle multiple tasks in a dynamic environment is essential. 

Additional Information

Why choose us?
It takes skill and passion to develop medicines the way we do. Don't worry - if you've got the passion part, we'll help you develop the skills you need to enhance every aspect of your career in the clinical research industry.
We've got an attitude at INC: "Can do, I own it." Absolutely everyone has ownership of what they do here. And because we're given the freedom and responsibility to really own our projects, we can take them to new levels. And that means we can take our careers wherever we want them, too.
"We were ranked "Top CRO" to work with in the CenterWatch 2013 Investigative Site Relationship Survey (a biannual survey of over 2,000 sites worldwide)."
What happens next?

If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity.


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