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Statistical Programmer 2 Jobs (NOW HIRING)

LivaNova

Statistical Programmer II

Austin, TX

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Dallas, TX · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

Gilead Sciences, Inc.

Statistical Programmer II

$107K - $138K/yr

Statistical programmers work collaboratively with internal colleagues and external vendors to ... Master's and 2 years of relevant experience OR * Bachelor's and 4 years of relevant experience ...

LivaNova

Statistical Programmer II

Houston, TX

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Minneapolis, MN · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Atlanta, GA

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Boston, MA

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Phoenix, AZ

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Raleigh, NC · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

KG Tiger

Statistical Programmer

Plymouth Meeting, PA · On-site

A design company that blends technology, creativity and engineering to help customers transform ... D. in Statistics, Mathematics or related field with two to five years of experience OR a Bachelor ...

Vrtx

Principal Statistical Programmer

Boston, MA · Remote

$149K - $223K/yr

The Principal Statistical Programmer works with management to delegate tasks appropriately, track ... to two days per week; or select 3. On-Site : work five days per week on-site with ad hoc ...

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Statistical Programmer 2 information

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$147.3K

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How much do statistical programmer 2 jobs pay per year?

As of Jun 20, 2026, the average yearly pay for statistical programmer 2 in the United States is $147,292.00, according to ZipRecruiter salary data. Most workers in this role earn between $125,000.00 and $160,000.00 per year, depending on experience, location, and employer.

How does a Statistical Programmer 2 typically collaborate with biostatisticians and clinical teams during a clinical trial project?

As a Statistical Programmer 2, you will frequently work closely with biostatisticians to implement statistical analysis plans, ensuring that data outputs meet regulatory standards and project specifications. Collaboration with clinical teams is also essential for clarifying data requirements, resolving discrepancies, and understanding study protocols. Effective communication and teamwork are crucial, as you may be responsible for translating statistical methods into programming code and explaining technical outputs to non-programmers. This collaborative environment provides opportunities to expand both your technical and interpersonal skills.

What are the key skills and qualifications needed to thrive as a Statistical Programmer 2, and why are they important?

To thrive as a Statistical Programmer 2, you need a strong background in statistics, data analysis, and programming languages such as SAS or R, usually supported by a degree in statistics, mathematics, or a related field. Experience with clinical trial data standards (like CDISC SDTM/ADaM), regulatory submission requirements, and data management systems is typically expected. Attention to detail, strong problem-solving skills, and effective communication are essential soft skills that help ensure accuracy and collaboration. These competencies are vital for delivering reliable statistical outputs and supporting successful clinical research and regulatory submissions.

What are Statistical Programmer 2s?

A Statistical Programmer 2 is a mid-level professional who specializes in writing and managing computer programs to analyze and process data, often in clinical research or pharmaceutical settings. They are responsible for generating statistical tables, listings, and figures, as well as validating data and ensuring compliance with regulatory standards. Typically, they work with software like SAS or R and collaborate closely with statisticians, data managers, and clinical teams to support data-driven decision-making. Their role requires a solid understanding of statistical methodologies, programming skills, and industry regulations.
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Statistical Programmer 2 jobs near you

Statistical Programmer II

Ruri Software Technologies LLC

Tampa, FL • On-site

Full-time

Posted yesterday

Job description

Role: Statistical Programmer II
Location : Tampa, Florida
Job Duties:
Roles and responsibilities she perfomed as a Statistical Programmer I/ Sas Programmer I from
Sep2019 - Jan2021 Includes the follows:
Provide statistical programming support for the reporting of clinical trial results of Phase 1
and Phase 2
Experience working with systems used within the Clinical Trial process.
Generated program as per STDM standards and Documentation of SAS code, log, Output
and report as per SOP guidelines.
Performed CDISC Mapping for Ongoing clinical trials and classified data into domains.
understanding with CDISC SDTM Implementation Guide v3.1.2/ v3.1.3 and SDTM
Model.
Proficient in generating clinical reports for safety analysis in the form of tables and listings.
Developed reports for safety as per study requirements debugging SAS errors and
identifying issues producing reports or analysis data sets and SAS data sets.
Roles and responsibilities she perfomed as a Statistical Programmer II/ Sas Programmer II from
feb2021 - Dec2022 Includes the follows:
Experienced in Writing statistical programs using SAS and R as per requests from internal
or external clients and reviewing the statistical analysis plan (SAP), SDRG and ADRG.
Handling of multiple Projects of client data to analyze Phase II and Phase III Clinical trials
data in various therapeutic areas like Hematology, endocrinology, Dermatology,
Gastroenterology, Immunology, Neurology and Virology to provide statistical
programming by using SAS tools such as SAS/MACROS, SAS/SQL and R experience for
the reporting of clinical trial results.
Involved in error handling, fixing bugs, and overcoming the challenges faced while
developing the code of specified structure of Tables and listings through creating Macros
and macro variables.
Experienced in data validation and data cleaning and worked understanding with CDISC
SDTM Implementation Guide v3.2/v3.3 and SDTM Model checks (through specifications) on
clinical trial datasets and QC of Statistical/ Programming outputs like Analysis Datasets and
aCRF (Case Report Form).
Experienced in creating reports using proc report and derived data sets (SDTM, CDISC,
ADAM) and Generated Define.xml output for FDA regulatory submissions.
Created efficacy customize reports for FDA regulatory submissions and develop to
maintain SAS programs to create SDTM and Adam datasets and created Tables and
Figures to support clinical trials.
Track clinical trial milestones for statistical programming deliverables.
Ensure compliance with SOPs/Guidelines, ICH-GCP, and any other applicable local and
international regulations, and participate in internal/external audits and regulatory
inspections as required.
Analyzed and validated data sets and SAS outputs with other programmer's outputs and
mockups in SAP using PROC COMPARE, PROC CONTENTS and PROC FREQ. Created
formats for the coded data and used PROC SQL for data validation.

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