Principal Statistical Programmer (US, CAD, UK only) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at ...
Principal Statistical Programmer (US, CAD, UK only) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at ...
Principal Statistical Programmer (US, CAD, UK only) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at ...
Principal Statistical Programmer (US, CAD, UK only) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at ...
Principal Statistical Programmer (US, CAD, UK only) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at ...
Principal Statistical Programmer (US, CAD, UK only) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at ...
Principal Statistical Programmer (US, CAD, UK only) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at ...
Principal Statistical Programmer (US, CAD, UK only) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at ...
Principal Statistical Associate - Biostatistician We are seeking a Principal Statistical Associate ... Oversee and consult on analytical programming, data management, and quality control. * Conduct ...
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Principal Statistical Associate - Biostatistician We are seeking a Principal Statistical Associate ... Oversee and consult on analytical programming, data management, and quality control. * Conduct ...
The principal statistical programmer will partner with statisticians to solve problems; reduce the amount of programming task being completed by statisticians to facilitate an increase in efficiency ...
The principal statistical programmer will partner with statisticians to solve problems; reduce the amount of programming task being completed by statisticians to facilitate an increase in efficiency ...
The principal statistical programmer will partner with statisticians to solve problems; reduce the amount of programming task being completed by statisticians to facilitate an increase in efficiency ...
The principal statistical programmer will partner with statisticians to solve problems; reduce the amount of programming task being completed by statisticians to facilitate an increase in efficiency ...
The principal statistical programmer will partner with statisticians to solve problems; reduce the amount of programming task being completed by statisticians to facilitate an increase in efficiency ...
The principal statistical programmer will partner with statisticians to solve problems; reduce the amount of programming task being completed by statisticians to facilitate an increase in efficiency ...
Principal Scientist, Stat. Programming- Early Oncology Development (Hybrid)
Rahway, NJ · On-site
$173.20 - $272.60/hr
The principal statistical programmer will partner with statisticians to solve problems; reduce the amount of programming task being completed by statisticians to facilitate an increase in efficiency ...
Principal Scientist, Stat. Programming- Early Oncology Development (Hybrid)
Rahway, NJ · On-site
$173.20 - $272.60/hr
The principal statistical programmer will partner with statisticians to solve problems; reduce the amount of programming task being completed by statisticians to facilitate an increase in efficiency ...
The principal statistical programmer will partner with statisticians to solve problems; reduce the amount of programming task being completed by statisticians to facilitate an increase in efficiency ...
The principal statistical programmer will partner with statisticians to solve problems; reduce the amount of programming task being completed by statisticians to facilitate an increase in efficiency ...
Principal / Associate Director, Statistical Programming
Conshohocken, PA · On-site
$180 - $219/hr
The Principal / Associate Director Statistical Programmer is an individual contributor responsible for leading and/or supporting multiple programming activities for Madrigal Pharmaceuticals across ...
Principal / Associate Director, Statistical Programming
Conshohocken, PA · On-site
$180 - $219/hr
The Principal / Associate Director Statistical Programmer is an individual contributor responsible for leading and/or supporting multiple programming activities for Madrigal Pharmaceuticals across ...
Make your mark for patients We are looking for a Principal Statistical Methodologist who is curious ... Strong statistical programming skills (R preferred; equivalent tools considered). * Sound knowledge ...
Make your mark for patients We are looking for a Principal Statistical Methodologist who is curious ... Strong statistical programming skills (R preferred; equivalent tools considered). * Sound knowledge ...
Make your mark for patients We are looking for a Principal Statistical Methodologist who is curious ... Strong statistical programming skills (R preferred; equivalent tools considered). * Sound knowledge ...
Make your mark for patients We are looking for a Principal Statistical Methodologist who is curious ... Strong statistical programming skills (R preferred; equivalent tools considered). * Sound knowledge ...
Position requires 14+ years of Statistical Programming experience with exploratory-stage oncology clinical trials, providing programming support and oversight of one or more clinical programs (early ...
Position requires 14+ years of Statistical Programming experience with exploratory-stage oncology clinical trials, providing programming support and oversight of one or more clinical programs (early ...
Position requires 14+ years of Statistical Programming experience with exploratory-stage oncology clinical trials, providing programming support and oversight of one or more clinical programs (early ...
Position requires 14+ years of Statistical Programming experience with exploratory-stage oncology clinical trials, providing programming support and oversight of one or more clinical programs (early ...
Associate Principal Scientist, Statistical Programming
$144K - $224K/yr
Associate Principal Scientist, Statistical Programming - Rahway, NJ: -Lead statistical programming activities for multiple and/or complex late-stage clinical trial development programs.Develop and ...
Associate Principal Scientist, Statistical Programming
$144K - $224K/yr
Associate Principal Scientist, Statistical Programming - Rahway, NJ: -Lead statistical programming activities for multiple and/or complex late-stage clinical trial development programs.Develop and ...
Associate Principal Scientist, Statistical Programming
$144K - $224K/yr
Associate Principal Scientist, Statistical Programming - Rahway, NJ: * Lead statistical programming activities for multiple and/or complex late-stage clinical trial development programs. * Develop ...
Associate Principal Scientist, Statistical Programming
$144K - $224K/yr
Associate Principal Scientist, Statistical Programming - Rahway, NJ: * Lead statistical programming activities for multiple and/or complex late-stage clinical trial development programs. * Develop ...
Associate Principal Scientist, Statistical Programming
Rahway, NJ · On-site
$144K - $224K/yr
Associate Principal Scientist, Statistical Programming - Rahway, NJ: * Lead statistical programming activities for multiple and/or complex late-stage clinical trial development programs. * Develop ...
Associate Principal Scientist, Statistical Programming
Rahway, NJ · On-site
$144K - $224K/yr
Associate Principal Scientist, Statistical Programming - Rahway, NJ: * Lead statistical programming activities for multiple and/or complex late-stage clinical trial development programs. * Develop ...
The Principal / Associate Director Statistical Programmer is an individual contributor responsible for leading and/or supporting multiple programming activities for Madrigal Pharmaceuticals across ...
The Principal / Associate Director Statistical Programmer is an individual contributor responsible for leading and/or supporting multiple programming activities for Madrigal Pharmaceuticals across ...
The Principal / Associate Director Statistical Programmer is an individual contributor responsible for leading and/or supporting multiple programming activities for Madrigal Pharmaceuticals across ...
The Principal / Associate Director Statistical Programmer is an individual contributor responsible for leading and/or supporting multiple programming activities for Madrigal Pharmaceuticals across ...
Principal Statistical Programmer information
See salary details
$55.77 - $61.32
7% of jobs
$61.32 - $66.87
7% of jobs
$66.87 - $72.42
8% of jobs
$72.91 is the 25th percentile. Wages below this are outliers.
$72.42 - $77.97
21% of jobs
The median wage is $79.88 / hr.
$77.97 - $83.52
17% of jobs
$83.52 - $89.07
9% of jobs
$93.79 is the 75th percentile. Wages above this are outliers.
$89.07 - $94.62
5% of jobs
$94.62 - $100.17
6% of jobs
$100.17 - $105.73
6% of jobs
$105.73 - $111.28
3% of jobs
$111.28 - $116.83
8% of jobs
$55
$84
$116
How much do principal statistical programmer jobs pay per hour?
What is a principal statistical programmer?
A Principal Statistical Programmer is a senior-level professional responsible for developing, validating, and maintaining statistical programs used in clinical trials and regulatory submissions. They ensure data accuracy, adherence to industry standards (such as CDISC), and compliance with regulatory requirements. They collaborate with statisticians, data managers, and clinical teams to analyze and report trial results. Additionally, they may mentor junior programmers and contribute to process improvements in statistical programming workflows.
What are the key skills and qualifications needed to thrive in the principal statistical programmer position, and why are they important?
To thrive as a Principal Statistical Programmer, you need advanced expertise in statistical programming (typically with SAS or R), a strong understanding of clinical trial data, and a degree in a relevant field such as statistics, mathematics, or computer science. Familiarity with CDISC standards (SDTM, ADaM), regulatory submission requirements, and project management tools is highly valued, and certifications like SAS Certified Advanced Programmer can be advantageous. Leadership, problem-solving, attention to detail, and excellent communication skills are important for managing complex projects and collaborating across multidisciplinary teams. These skills collectively ensure accuracy, regulatory compliance, and successful delivery of statistical programming support within clinical research environments.
What are the typical daily responsibilities of a principal statistical programmer in a clinical research setting?
As a Principal Statistical Programmer, your daily responsibilities often include developing, validating, and maintaining complex statistical programs to support clinical trial data analysis and regulatory submissions. You may lead programming teams, mentor junior staff, and act as a technical expert on study projects, collaborating closely with statisticians, data managers, and clinical teams. The role frequently involves reviewing statistical analysis plans (SAPs), generating data listings and summary tables, and ensuring adherence to industry standards such as CDISC. Effective communication and time management are key, as you’ll often work on multiple projects simultaneously, balancing deliverables and troubleshooting technical challenges. This position offers diverse, impactful work where your expertise significantly contributes to the integrity and success of clinical research programs.

Principal Statistical Programmer (US, CAD, UK only)
Bridgewater, NJ • On-site
Other
Re-posted 3 days ago
Syneos Health rating
8.1
Based on 22 frontline employees who took The Breakroom Quiz
38th of 86 rated pharmaceutical
Job description
Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:
Why Syneos Health
* We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
* We are committed to building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
* We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities
**Must be located in US, CAD, UK with no sponsorship needs
**Hiring at Sr level only for NA
**Graph experience, plus experience writing specifications for ADaM datasets is required.
* Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications.
* Works to ensure that outputs meet quality standards and project requirements.
* Performs validation programming and works with other Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings.
* Keeps project team members informed of programming progress and issues requiring their attention.
* Follow applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH).
* Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs ensuring inspection readiness.
* Manages scheduling and time constraints across multiple projects at a time, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload.
* Develops specifications for datasets and outputs of any complexity according to statistical and sponsor requirements. Anticipates and addresses potential programming issues, reflects forethought, establishes the basis for efficient programming and accurately defines allvariables to be accepted by peer review and sponsor/requestor with little rework.
* Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others.
* Conducts effective internal meetings (appropriate in format, frequency and attendance). Distributes relevant information in advance. Ensures minutes are promptly and accurately distributed. Follows action items through to completion, and maintains order and focus of meetings, working toward consensus.
* Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business.
* Negotiates and establishes accurate time estimates for completion of study programming activities with internal team members and statistical programming management, and completes project programming activities within timeframe allotted.
* Acts as the lead statistical programmer. Directs the programming activities of other programming personnel and monitors progress on programming deliverables.
* Reviews project documentation such as Statistical Analysis Plan, mock shells, programming specifications, annotated CRFs, and SAS database design. Provides feedback to the appropriate project team members which reflects forethought and reduces inefficiencies in programming activities.
* Participates in sponsor meetings, kickoff meetings, and bid defense meetings as statistical programming representative, as required by sponsor.
* Contributes to the mentoring of programming personnel through developing training courses, presenting training materials, reviewing work, and providing feedback or guiding new associates in process.
* Transfers deliverables.
* Performs other work-related duties as assigned.
* Minimal travel may be required
Qualifications
* Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of degree, an equivalent combination of education and demonstrated programming experience.
* Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.
* Excellent written and verbal communication skills.
* Ability to read, write, speak and understand English.
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
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About Syneos Health
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Industry
Scientific research and development services and marketing
Company size
10,000+ Employees
Headquarters location
Morrisville, NC, US