Statistical Programmer II
$90K - $100K/yr
The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.
$90K - $100K/yr
The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.
$90K - $100K/yr
The statistical programming team develops datasets from our clinical trials and delivers tables ... Provide input into SAP, analysis specifications, and data presentations for clinical trials.
Lexington, MA · On-site +1
The Senior Statistical Programmer is responsible for developing, testing, maintaining, validating ... Generate analysis datasets, tables, figures, and listings for clinical trials, regulatory ...
New
Lexington, MA · On-site +1
The Senior Statistical Programmer is responsible for developing, testing, maintaining, validating ... Generate analysis datasets, tables, figures, and listings for clinical trials, regulatory ...
New
Andover, MA · On-site +1
The Senior Statistical Programmer is responsible for developing, testing, maintaining, validating ... Generate analysis datasets, tables, figures, and listings for clinical trials, regulatory ...
New
Andover, MA · On-site +1
The Senior Statistical Programmer is responsible for developing, testing, maintaining, validating ... Generate analysis datasets, tables, figures, and listings for clinical trials, regulatory ...
New
Marlborough, MA · On-site +1
The Senior Statistical Programmer is responsible for developing, testing, maintaining, validating ... Generate analysis datasets, tables, figures, and listings for clinical trials, regulatory ...
New
Marlborough, MA · On-site +1
The Senior Statistical Programmer is responsible for developing, testing, maintaining, validating ... Generate analysis datasets, tables, figures, and listings for clinical trials, regulatory ...
New
Woburn, MA · On-site +1
The Senior Statistical Programmer is responsible for developing, testing, maintaining, validating ... Generate analysis datasets, tables, figures, and listings for clinical trials, regulatory ...
New
Woburn, MA · On-site +1
The Senior Statistical Programmer is responsible for developing, testing, maintaining, validating ... Generate analysis datasets, tables, figures, and listings for clinical trials, regulatory ...
New
Principal Statistical Programmer, Biometrics Who we are: At Agios, we are fueled by connections to ... Review statistical analyses plans and case report forms. * Ensure documentation is maintained to ...
Principal Statistical Programmer, Biometrics Who we are: At Agios, we are fueled by connections to ... Review statistical analyses plans and case report forms. * Ensure documentation is maintained to ...
Principal Statistical Programmer, Biometrics Who we are: At Agios, we are fueled by connections to ... Review statistical analyses plans and case report forms. * Ensure documentation is maintained to ...
Principal Statistical Programmer, Biometrics Who we are: At Agios, we are fueled by connections to ... Review statistical analyses plans and case report forms. * Ensure documentation is maintained to ...
Boston, MA · Remote
$149K - $223K/yr
The Principal Statistical Programmer works with management to delegate tasks appropriately, track ... Creates all files, documents, and analyses necessary to support an electronic submission in eCTD ...
Boston, MA · Remote
$149K - $223K/yr
The Principal Statistical Programmer works with management to delegate tasks appropriately, track ... Creates all files, documents, and analyses necessary to support an electronic submission in eCTD ...
Boston, MA · On-site
$149K - $223K/yr
The Principal Statistical Programmer works with management to delegate tasks appropriately, track ... Creates all files, documents, and analyses necessary to support an electronic submission in eCTD ...
Boston, MA · On-site
$149K - $223K/yr
The Principal Statistical Programmer works with management to delegate tasks appropriately, track ... Creates all files, documents, and analyses necessary to support an electronic submission in eCTD ...
Requirements will be identified according to a Statistical Analysis Plan andprogramming ... Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools ...
Requirements will be identified according to a Statistical Analysis Plan andprogramming ... Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools ...
Requirements will be identified according to a Statistical Analysis Plan andprogramming ... Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools ...
Requirements will be identified according to a Statistical Analysis Plan andprogramming ... Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools ...
Cambridge, MA · On-site
$181K - $244K/yr
The Associate Director, Statistical Programming is responsible for statistical programming ... Works closely with Biostatistics to implement statistical analysis of clinical trial data, working ...
Cambridge, MA · On-site
$181K - $244K/yr
The Associate Director, Statistical Programming is responsible for statistical programming ... Works closely with Biostatistics to implement statistical analysis of clinical trial data, working ...
$168K - $210K/yr
Perform Data analysis, statistical analysis, generate safety and efficacy tables, listings and ... Support End-to-End Statistical Programming using SAS * Ability to generate documents / files ...
$168K - $210K/yr
Perform Data analysis, statistical analysis, generate safety and efficacy tables, listings and ... Support End-to-End Statistical Programming using SAS * Ability to generate documents / files ...
Marlborough, MA · On-site
$168K - $210K/yr
Perform Data analysis, statistical analysis, generate safety and efficacy tables, listings and ... Support End-to-End Statistical Programming using SAS * Ability to generate documents / files ...
Marlborough, MA · On-site
$168K - $210K/yr
Perform Data analysis, statistical analysis, generate safety and efficacy tables, listings and ... Support End-to-End Statistical Programming using SAS * Ability to generate documents / files ...
$184K - $198K/yr
D) with strong analytical skills * Minimum 8+ years experiences in pharmaceutical/biotech and/or ... Function as lead programmer to coordinate all activities related to study or project level ...
$184K - $198K/yr
D) with strong analytical skills * Minimum 8+ years experiences in pharmaceutical/biotech and/or ... Function as lead programmer to coordinate all activities related to study or project level ...
Waltham, MA · On-site
$184K - $198K/yr
Function as lead programmer to coordinate all activities related to study or project level ... D) with strong analytical skills * Minimum 8+ years experiences in pharmaceutical/biotech and/or ...
Waltham, MA · On-site
$184K - $198K/yr
Function as lead programmer to coordinate all activities related to study or project level ... D) with strong analytical skills * Minimum 8+ years experiences in pharmaceutical/biotech and/or ...
Waltham, MA · On-site
$184K - $198K/yr
Function as lead programmer to coordinate all activities related to study or project level ... D) with strong analytical skills * Minimum 8+ years experiences in pharmaceutical/biotech and/or ...
Waltham, MA · On-site
$184K - $198K/yr
Function as lead programmer to coordinate all activities related to study or project level ... D) with strong analytical skills * Minimum 8+ years experiences in pharmaceutical/biotech and/or ...
$184K - $198K/yr
D) with strong analytical skills * Minimum 8+ years experiences in pharmaceutical/biotech and/or ... Function as lead programmer to coordinate all activities related to study or project level ...
$184K - $198K/yr
D) with strong analytical skills * Minimum 8+ years experiences in pharmaceutical/biotech and/or ... Function as lead programmer to coordinate all activities related to study or project level ...
Cambridge, MA · On-site +1
Develop and execute statistical analysis and reporting deliverables (tables, figures and listings ... Provide programming support for building integrated summary of safety/efficacy datasets and ...
Cambridge, MA · On-site +1
Develop and execute statistical analysis and reporting deliverables (tables, figures and listings ... Provide programming support for building integrated summary of safety/efficacy datasets and ...
Boston, MA · On-site
$151K - $172K/yr
Independently implement routine and non-standard analysis algorithms for assigned projects or studies * Collaborate with statisticians, local and CRO programmers to define and implement analysis ...
Boston, MA · On-site
$151K - $172K/yr
Independently implement routine and non-standard analysis algorithms for assigned projects or studies * Collaborate with statisticians, local and CRO programmers to define and implement analysis ...
$67.5K - $76.5K
19% of jobs
$80.1K is the 25th percentile. Wages below this are outliers.
$76.5K - $85.5K
16% of jobs
$85.5K - $94.4K
9% of jobs
The median wage is $98K / yr.
$94.4K - $103.4K
16% of jobs
$103.4K - $112.4K
0% of jobs
$121.3K is the 75th percentile. Wages above this are outliers.
$112.4K - $121.3K
16% of jobs
$121.3K - $130.3K
0% of jobs
$130.3K - $139.2K
6% of jobs
$139.2K - $148.2K
6% of jobs
$148.2K - $157.2K
6% of jobs
$157.2K - $166.1K
6% of jobs
$67.5K
$109.7K
$166.1K
| Aspect | Statistical Programmer Analyst | Data Analyst |
|---|---|---|
| Required Credentials | Bachelor's in Statistics, Computer Science, or related field; experience with SAS, R, or Python | Bachelor's in Statistics, Data Science, or related field; proficiency in Excel, SQL, and visualization tools |
| Work Environment | Pharmaceutical, clinical research, or healthcare industries; focus on programming and statistical analysis | Various industries including finance, marketing, healthcare; focus on data interpretation and reporting |
| Employer & Industry Usage | Common in clinical trials, biotech, pharma companies | Widely used across multiple sectors including business, finance, and healthcare |
The main difference is that a Statistical Programmer Analyst primarily focuses on programming and analyzing clinical or research data using statistical software, while a Data Analyst often handles broader data interpretation and reporting across various industries. Both roles require similar technical skills but differ in industry focus and specific responsibilities.

$90K - $100K/yr
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 8 days ago
As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow-because at LivaNova, we don't just treat conditions - we aspire to alter the course of lives.
Come join a great company and be part of a dynamic, growing team of programmers. Put your expertise to great use as we improve our programming standards and processes to develop best-in-class programming outputs. 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 therapies, as well as togenerate evidence for marketed devices. This talented team also supports additional programming activities for clinical operations and other areas of the company, including R&D and Quality.
The Role
The Statistical Programmer will support programming activities for multiple projects on clinical study reports and publications.
Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of Statistics & Data Management.
Collaborate with Statistics, Data Management, Clinical, and vendor teams to clarify requirements and resolve data or programming issues.
Develop, validate, and maintain SAS programs in accordance with study requirements, internal standards, and SOPs
Contribute to the creation, validation, and documentation of SDTM and ADaM datasets.
Responsible for producing programming outputs, validation, and related documentation to ensure accuracy, consistency, and traceability.
Ensure deliverables meet expectations in terms of timelines and quality, regulatory and key user group requirements (e.g., CDISC), operational efficiency, and alignment with the study's clinical and statistical objectives.
Provide input into SAP, analysis specifications, and data presentations for clinical trials.
Support ongoing workflow modernization, migration activities, and standardization initiatives.
Participate in process improvement activities related to programming efficiency, quality, and standardization.
Minimum Requirements
Bachelor's degree or higher in statistics, mathematics, computer science, life sciences, data science, or related field.
Relevant experience in clinical trial programming, clinical data analysis, statistical programming, or regulated data environments.
Strong SAS programming skills, including data step, procedures, macros, and debugging.
Ability to write clear, validated, reusable, and well-documented code.
Understanding of programming quality control, validation, and traceability expectations.
Working knowledge of CDISC standards, especially SDTM and ADaM.
Ability to support dataset creation, validation, listings, tables, figures, and ad hoc analyses.
Understanding of clinical trial data flow from data collection to analysis/reporting.
Strong attention to detail and quality.
Ability to work independently on assigned tasks with appropriate guidance.
Good communication skills and ability to collaborate with Statistics, Data Management, Clinical, and external vendors.
Ability to manage priorities and timelines in a changing project environment.
Desired Qualifications
Experience with R, Python, SQL, Git, or other modern programming/version control tools.
Experience with SAS Enterprise Guide or other SAS-based clinical programming environments.
Experience supporting medical device, neuromodulation, or cardiovascular/respiratory studies.
Familiarity with data visualization, dashboards, automation, or workflow improvement.
Experience working with vendors or cross-functional global teams.
Understanding of controlled programming environments, SOPs, and audit-ready documentation.
Pay Transparency
A reasonable estimate of the annual base salary for this position is $90,000 - $100,000 plus discretionary annual bonus. Pay ranges may vary by location and are awarded based on experience.
Employee benefits include:
Health benefits - Medical, Dental, Vision
Personal and Vacation Time
Retirement & Savings Plan (401K)
Employee Stock Purchase Plan
Training & Education Assistance
Bonus Referral Program
Service Awards
Employee Recognition Program
Flexible Work Schedules
Valuing different backgrounds:
LivaNova values equality and diversity. We are committed to ensuring that our recruitment process is fair, transparent and free from unlawful discrimination. Our selection process is driven by the key demands/requirements for the role rather than bias or discrimination on the basis of a candidate's sex, gender identity, age, marital status, veteran status, non-job-related disability/handicap or medical condition, family status, sexual orientation, religion, color, ethnicity, race or any other legally protected classification.
Notice to third party agencies:
Please note that we do not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Recruitment Services Agreement, we will not consider, or agree to, payment of any referral compensation or recruiter fee. In the event that a recruiter or agency submits a resume or candidate without a previously signed agreement, we explicitly reserve the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency.
Beware of Job Scams:
Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons posing as LivaNova recruiters or employees. The scammers may attempt to solicit confidential, personal information, such as a social security number, or your financial information. LivaNova will never ask for fees prior/during/after the application process, nor will we ask for banking details or personal financial information in return for the assurance of employment. If you are concerned that an offer of employment might be a scam or that the recruiter is not legitimate, please verify by searching for "See Open Jobs" onhttps://www.livanova.com/en-us/careers, and check that all recruitment emails come from an @livanova.com email address.