Statistical Programmer II
$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 ...
$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 ...
$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 ...
Principal Statistical Programmer, Biometrics At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that sparks bold thinking and ...
Principal Statistical Programmer, Biometrics At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that sparks bold thinking and ...
Principal Statistical Programmer, Biometrics Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that sparks bold ...
Principal Statistical Programmer, Biometrics Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that sparks bold ...
Principal Statistical Programmer, Biometrics Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that sparks bold ...
Principal Statistical Programmer, Biometrics Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that sparks bold ...
The Biometrics Quality Team provides leadership and support for the Global Biometrics department, which consists of Data Management, Biostatistics and Statistical Programming. The Sr. Associate ...
The Biometrics Quality Team provides leadership and support for the Global Biometrics department, which consists of Data Management, Biostatistics and Statistical Programming. The Sr. Associate ...
Cambridge, MA · On-site
$109K - $179K/yr
Principal Statistical Programmer A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies. In this role, a typical ...
Cambridge, MA · On-site
$109K - $179K/yr
Principal Statistical Programmer A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies. In this role, a typical ...
Boston, MA · On-site
The Contract Lead Programmer serves as a senior, hands-on programmer responsible for managing statistical programming activities across multiple clinical trials and therapeutic areas. The role ...
Boston, MA · On-site
The Contract Lead Programmer serves as a senior, hands-on programmer responsible for managing statistical programming activities across multiple clinical trials and therapeutic areas. The role ...
A principal statistical programmer provides timely support to the study team on all programming matters according to theproject strategies. In this role, a typical day might include: As an integral ...
A principal statistical programmer provides timely support to the study team on all programming matters according to theproject strategies. In this role, a typical day might include: As an integral ...
Needham, MA · On-site
$165K - $190K/yr
Associate Director, Statistical Programming Job Duties: * Lead design and development SAS programs and the programming specifications for producing and validating CDISC ADaM datasets to support the ...
Needham, MA · On-site
$165K - $190K/yr
Associate Director, Statistical Programming Job Duties: * Lead design and development SAS programs and the programming specifications for producing and validating CDISC ADaM datasets to support the ...
Needham, MA · On-site +1
$165K - $190K/yr
Associate Director, Statistical Programming Job Duties: * Lead design and development SAS programs and the programming specifications for producing and validating CDISC ADaM datasets to support the ...
Needham, MA · On-site +1
$165K - $190K/yr
Associate Director, Statistical Programming Job Duties: * Lead design and development SAS programs and the programming specifications for producing and validating CDISC ADaM datasets to support the ...
Marlborough, MA · On-site
$168K - $210K/yr
Responsible for planning and tracking statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings ...
Marlborough, MA · On-site
$168K - $210K/yr
Responsible for planning and tracking statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings ...
Waltham, MA · On-site
$184K - $198K/yr
Function as lead programmer to coordinate all activities related to study or project level statistical programming activities. * Design and develop programming specifications and SAS programs for ...
Waltham, MA · On-site
$184K - $198K/yr
Function as lead programmer to coordinate all activities related to study or project level statistical programming activities. * Design and develop programming specifications and SAS programs for ...
Marlborough, MA · On-site
$168K - $210K/yr
Responsible for planning and tracking statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings ...
Marlborough, MA · On-site
$168K - $210K/yr
Responsible for planning and tracking statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings ...
Waltham, MA · On-site
$184K - $198K/yr
Function as lead programmer to coordinate all activities related to study or project level statistical programming activities. * Design and develop programming specifications and SAS programs for ...
Waltham, MA · On-site
$184K - $198K/yr
Function as lead programmer to coordinate all activities related to study or project level statistical programming activities. * Design and develop programming specifications and SAS programs for ...
Waltham, MA · On-site
$184K - $198K/yr
Function as lead programmer to coordinate all activities related to study or project level statistical programming activities. * Design and develop programming specifications and SAS programs for ...
Waltham, MA · On-site
$184K - $198K/yr
Function as lead programmer to coordinate all activities related to study or project level statistical programming activities. * Design and develop programming specifications and SAS programs for ...
Waltham, MA · On-site
$184K - $198K/yr
Function as lead programmer to coordinate all activities related to study or project level statistical programming activities. * Design and develop programming specifications and SAS programs for ...
Waltham, MA · On-site
$184K - $198K/yr
Function as lead programmer to coordinate all activities related to study or project level statistical programming activities. * Design and develop programming specifications and SAS programs for ...
Cambridge, MA · On-site +1
The Opportunity Reporting into the Statistical Programming function, you will be responsible for providing hands-on programming support and technical guidance on clinical trials and regulatory ...
Cambridge, MA · On-site +1
The Opportunity Reporting into the Statistical Programming function, you will be responsible for providing hands-on programming support and technical guidance on clinical trials and regulatory ...
Beam is looking for a highly talented and motivated Associate Director, Statistical Programming, to join our growing Statistical Programming team in the Biometrics department. The senior manager will ...
Beam is looking for a highly talented and motivated Associate Director, Statistical Programming, to join our growing Statistical Programming team in the Biometrics department. The senior manager will ...
Cambridge, MA · On-site
$95K - $130K/yr
You will lead a study team of statistical programmers to accomplish tasks and communicate issues, as necessary, to line management. This includes communication and quality oversight of the vendor.
Cambridge, MA · On-site
$95K - $130K/yr
You will lead a study team of statistical programmers to accomplish tasks and communicate issues, as necessary, to line management. This includes communication and quality oversight of the vendor.
Cambridge, MA · On-site
$116K - $163K/yr
You will lead a study team of statistical programmers to accomplish tasks and communicate issues, as necessary, to line management. This includes communication and quality oversight of the vendor.
Cambridge, MA · On-site
$116K - $163K/yr
You will lead a study team of statistical programmers to accomplish tasks and communicate issues, as necessary, to line management. This includes communication and quality oversight of the vendor.
$91.8K - $108K
3% of jobs
$108K - $124.3K
10% of jobs
$135.3K is the 25th percentile. Wages below this are outliers.
$124.3K - $140.5K
18% of jobs
The median wage is $156.8K / yr.
$140.5K - $156.8K
19% of jobs
$170.9K is the 75th percentile. Wages above this are outliers.
$156.8K - $173K
29% of jobs
$173K - $189.3K
10% of jobs
$189.3K - $205.5K
12% of jobs
$205.5K - $221.8K
0% of jobs
$221.8K - $238K
0% of jobs
$238K - $254.3K
0% of jobs
$254.3K - $270.5K
0% of jobs
$91.8K
$160K
$270.5K
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.
| Aspect | Statistical Programmer | Data Analyst |
|---|---|---|
| Required Credentials | Bachelor's in Statistics, Biostatistics, 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 data management | Various industries including finance, marketing, healthcare; focus on data interpretation and reporting |
| Employer & Industry Usage | Common in clinical trials, biotech, pharma companies | Used 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.

$90K - $100K/yr
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 20 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.