The senior statistical programmer will gather and interpret user requirements for programming requests, retrieve required data, transform data into analysis/modeling datasets, and develop tables ...
The senior statistical programmer will gather and interpret user requirements for programming requests, retrieve required data, transform data into analysis/modeling datasets, and develop tables ...
The senior programmer will be a key collaborator with statisticians, modelers, and colleagues in other related function areas.Primary Activities :Prepare compliant programming code for regulatory ...
New
The senior programmer will be a key collaborator with statisticians, modelers, and colleagues in other related function areas.Primary Activities :Prepare compliant programming code for regulatory ...
New
Sr R & SAS Programmer
Chesterbrook, PA · On-site
Sr SAS & R Programmer onsite in the Chesterbrook, PA area 3 days/week SUMMARY The contract Senior Statistical Programmer is a member of the Biometrics Department within the Research and Development ...
Sr R & SAS Programmer
Chesterbrook, PA · On-site
Sr SAS & R Programmer onsite in the Chesterbrook, PA area 3 days/week SUMMARY The contract Senior Statistical Programmer is a member of the Biometrics Department within the Research and Development ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides oversight and quality management of submission data standard deliverables for world-wide regulatory ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides oversight and quality management of submission data standard deliverables for world-wide regulatory ...
Role Overview We are seeking a highly experienced Senior Statistical Programmer / Clinical Data Architect with 15+ years of expertise in clinical data programming, CDISC standards, and cloud-based ...
Quick apply
Role Overview We are seeking a highly experienced Senior Statistical Programmer / Clinical Data Architect with 15+ years of expertise in clinical data programming, CDISC standards, and cloud-based ...
The senior manager will be responsible for developing and maintaining statistical programming functions within a therapeutic area to support various clinical studies and submissions to ensure ...
The senior manager will be responsible for developing and maintaining statistical programming functions within a therapeutic area to support various clinical studies and submissions to ensure ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides oversight and quality management of submission data standard deliverables for world-wide regulatory ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides oversight and quality management of submission data standard deliverables for world-wide regulatory ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides oversight and quality management of submission data standard deliverables for world-wide regulatory ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides oversight and quality management of submission data standard deliverables for world-wide regulatory ...
Position Title: Senior Manager, Statistical Programming Department: Clinical Data Sciences ... Serve as the lead programmer to reviews SAP, Data Presentation Plan, Table Shell to align with ...
Position Title: Senior Manager, Statistical Programming Department: Clinical Data Sciences ... Serve as the lead programmer to reviews SAP, Data Presentation Plan, Table Shell to align with ...
SAS Programmer
Jersey City, NJ · On-site
The role of the Senior Statistical Programmer is to perform statistical programming activities for all assigned Phase I-IV clinical studies. This position performs statistical programming for ...
SAS Programmer
Jersey City, NJ · On-site
The role of the Senior Statistical Programmer is to perform statistical programming activities for all assigned Phase I-IV clinical studies. This position performs statistical programming for ...
Beam is looking for a Senior Manager/Associate Director of statistical programming to join our growing Statistical Programming team in the Biometrics department. This individual will be responsible ...
Beam is looking for a Senior Manager/Associate Director of statistical programming to join our growing Statistical Programming team in the Biometrics department. This individual will be responsible ...
The Senior Manager of Statistical Programming will be responsible for leading Statistical ... Serve as the lead programmer to reviews SAP, Data Presentation Plan, Table Shell to align with ...
The Senior Manager of Statistical Programming will be responsible for leading Statistical ... Serve as the lead programmer to reviews SAP, Data Presentation Plan, Table Shell to align with ...
The Senior Statistical Programmer is a delivery focused role responsible for programming deliverables with quality and timeliness, following established standards and processes. * This position ...
Quick apply
The Senior Statistical Programmer is a delivery focused role responsible for programming deliverables with quality and timeliness, following established standards and processes. * This position ...
Sr. Manager, Statistical Programming
Boston, MA · On-site
$151K - $172K/yr
Role Summary The Sr Manager, Statistical Programming is responsible for the development of statistical programming on the study level by performing hands-on programming or oversight of outsourced ...
Sr. Manager, Statistical Programming
Boston, MA · On-site
$151K - $172K/yr
Role Summary The Sr Manager, Statistical Programming is responsible for the development of statistical programming on the study level by performing hands-on programming or oversight of outsourced ...
Senior Manager, Statistical Programming
Cambridge, MA · On-site
$155K - $190K/yr
The senior manager will be responsible for developing and maintaining statistical programming functions within a therapeutic area to support various clinical studies and submissions to ensure ...
Senior Manager, Statistical Programming
Cambridge, MA · On-site
$155K - $190K/yr
The senior manager will be responsible for developing and maintaining statistical programming functions within a therapeutic area to support various clinical studies and submissions to ensure ...
Job Title: Sr. Associate, Biometrics Quality Location: Cambridge, MA Duration: 12+ months ... Statistical Programming. The Sr. Associate, Biometrics Quality role will be responsible for:
Job Title: Sr. Associate, Biometrics Quality Location: Cambridge, MA Duration: 12+ months ... Statistical Programming. The Sr. Associate, Biometrics Quality role will be responsible for:
At least 8 years work experience in a Statistical (SAS) programming role preferably supporting ... Additional Information Richha Saini Senior Clinical/Scientific Recruiter 360 Mt. Kemble Avenue ...
At least 8 years work experience in a Statistical (SAS) programming role preferably supporting ... Additional Information Richha Saini Senior Clinical/Scientific Recruiter 360 Mt. Kemble Avenue ...
Senior Principal Statistical Programmer
$119K - $222K/yr
The Statistical Programming community at Novartis comprises of approximately 350 (internal) statistical programmers and belongs to the Advanced Quantitative Sciences (AQS) organization which also ...
Senior Principal Statistical Programmer
$119K - $222K/yr
The Statistical Programming community at Novartis comprises of approximately 350 (internal) statistical programmers and belongs to the Advanced Quantitative Sciences (AQS) organization which also ...
Senior Principal Statistical Programmer
$119K - $222K/yr
The Statistical Programming community at Novartis comprises of approximately 350 (internal) statistical programmers and belongs to the Advanced Quantitative Sciences (AQS) organization which also ...
Senior Principal Statistical Programmer
$119K - $222K/yr
The Statistical Programming community at Novartis comprises of approximately 350 (internal) statistical programmers and belongs to the Advanced Quantitative Sciences (AQS) organization which also ...
Senior Principal Statistical Programmer
$119K - $222K/yr
The Statistical Programming community at Novartis comprises of approximately 350 (internal) statistical programmers and belongs to the Advanced Quantitative Sciences (AQS) organization which also ...
Senior Principal Statistical Programmer
$119K - $222K/yr
The Statistical Programming community at Novartis comprises of approximately 350 (internal) statistical programmers and belongs to the Advanced Quantitative Sciences (AQS) organization which also ...
Senior Statistical Programmer information
See salary details
$82.5K - $90.2K
2% of jobs
$90.2K - $98K
7% of jobs
$98K - $105.7K
14% of jobs
$107K is the 25th percentile. Wages below this are outliers.
$105.7K - $113.4K
13% of jobs
$113.4K - $121.1K
7% of jobs
The median wage is $126.1K / yr.
$121.1K - $128.9K
11% of jobs
$128.9K - $136.6K
10% of jobs
$136.6K - $144.3K
9% of jobs
$145.2K is the 75th percentile. Wages above this are outliers.
$144.3K - $152K
9% of jobs
$152K - $159.8K
6% of jobs
$159.8K - $167.5K
10% of jobs
$82.5K
$128.3K
$167.5K
How much do senior statistical programmer jobs pay per year?
What is a Senior Statistical Programmer job?
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 key skills and qualifications needed to thrive in the Senior Statistical Programmer position, 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 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.

Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 3 days ago
Merck rating
7.8
Based on 50 frontline employees who took The Breakroom Quiz
41st of 71 rated pharmaceutical
Job description
In BARDS (Biostatistics and Research Decision Sciences), 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.
Summary
Responsibilities:
This position provides high quality statistical programming deliverables for global stakeholders in Early Development Statistics and PK/PD Modeling and Simulation spanning all our Company's therapeutic areas except oncology. The senior statistical programmer will gather and interpret user requirements for programming requests, retrieve required data, transform data into analysis/modeling datasets, and develop tables, listings and figures according to statistical/modeling analysis plan. The senior programmer will be a key collaborator with statisticians, modelers, and colleagues in other related function areas.
Primary Activities:
- Prepare compliant programming code for regulatory submissions including analysis/modeling datasets, tables, listings, figures and associated documentation
- Ensure programmatic traceability from data source to analysis/modeling result
- Support the development of programming standards to enable efficient and high-quality production of programming deliverables
Skills
Education and Minimum Requirement:
- BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS/R programming experience in a clinical trial environment OR
- MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years SAS/R programming experience in a clinical trial environment
Department Required Skills and Experience:
- Excellent communication (oral, written) skills, interpersonal skills and ability to negotiate and collaborate effectively
- Effective knowledge and experience in developing analysis and reporting deliverables for research and development projects (data, analyses, tables, graphics, listings)
- A project leader; completes tasks independently at project level
Position Specific Required Skills and Experience:
- Programming expertise with clinical endpoint data (efficacy and safety)
- Experience in CDISC SDTM and ADaM standards
- If owns SAS programming experience, significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH
- Designs and develops complex programming algorithms
- Ability to comprehend analysis plans which may describe methodology to be programmed; understanding of statistical terminology and concepts; Implements statistical methods not currently available through commercial software packages.
Preferred Skills and Experience:
- Programming expertise with pharmacokinetic data (raw concentration data, derived PK parameters)
- Familiarity with clinical pharmacology concepts and pharmacokinetics concepts
- Experience with at least one other software than SAS/R (e.g., Python, NONMEM)
- Good working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC)
- Utilizes and contributes to the development of standard departmental SAS macros
- Ability and interest to work across cultures and geographies
- Ability to complete statistical programming deliverables through the use of global outsource partner programming staff
- Active in professional societies
eligibleforERP
SPjobs
BARDS2020
VETJOBS
EBRG
Required Skills:
Accountability, Applied Engineering, Clinical Trials, Computer Science, Data Analysis, Data Management, Data Modeling, Mechatronics, Numerical Analysis, R Programming, Software Development, Stakeholder Relationship Management, Statistical Analysis Systems (SAS) Programming, Statistical Programming, Waterfall Model
Preferred Skills:
NONMEM, Pharmacokinetic Modeling, PKPD Modeling, Python (Programming Language), Translational Pharmacokinetics and Pharmacodynamics (PKPD)
Current Employees apply HERE
Current Contingent Workers apply HERE
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. Please click here if you need an accommodation during the application or hiring process.
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
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.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). 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:
06/24/2026
*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.
About Merck
Sourced by ZipRecruiter
Industry
Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
Rahway, NJ, US