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Senior Statistical Programmer Jobs in Guelph, ON

SAS programming and program validation * Review and QC of statistical deliverables (tables, listings, figures, etc.) * Perform statistical analysis and report results * Consult on experimental design ...

Position Summary The Senior Manufacturing Quality Engineer is a technical leader responsible for ... Statistical Engineering * Serve as the manufacturing statistical expert applying DOE, SPC, Cp/Cpk ...

Move Your Career Forward with DAC a Senior Data Scientist Who We Are We are DAC-a global full ... Expert-level proficiency in statistical programming (Python or R) with ability to write production ...

Senior Process Engineer Location: Cambridge, Ontario (On-site) Type: Full Time, Permanent Shift ... Apply statistical analysis, statistical process control, and data analytics to optimize process ...

The Senior / Lead Data Engineer will bepart of McKesson Decision Intelligence team, and ... Understanding oflarge database mining tools and statistical languagesutilizedto efficiently build ...

The Senior / Lead Data Engineer will bepart of McKesson Decision Intelligence team, and ... Understanding oflarge database mining tools and statistical languagesutilizedto efficiently build ...

Work at the intersection of large-scale data engineering, statistical modelling, and cutting-edge ... A "Day in the Life" of a Senior Data Engineer: * Design, develop, and maintain scalable, real-time ...

... As a Senior ML Developer on the team, you will be responsible for leading/contributing to the ... Perform statistical and data analysis and exploration to generate datasets for model training and ...

Quality Engineer, Senior Job Summary The Senior Quality Engineer works with production and ... Advanced knowledge of applying Statistical Process Control (SPC) concepts. * Understanding of ...

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Senior Statistical Programmer information

See Guelph, ON salary details

$77.5K

$112.1K

$150.2K

How much do senior statistical programmer jobs pay per year?

As of Aug 25, 2026, the average yearly pay for senior statistical programmer in Guelph, ON is $112,123.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,538.00 and $124,245.00 per year, depending on experience, location, and employer.

What is a senior statistical programmer?

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 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.

What are the key skills and qualifications needed to thrive as a senior statistical programmer, 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.

Infographic showing various Senior Statistical Programmer job openings in Guelph, ON as of August 2026, with employment types broken down into 1% Internship, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $112,123 per year, or $53.9 per hour.

Senior Statistician

PSI CRO

Toronto, ON • On-site

Full-time

Posted 24 days ago


Job description

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

In this role, you will:

  • Lead all biostatistics activities related to clinical trials as responsible project statistician
  • Communicate with project teams, clients and vendors on statistical questions
  • Develop and review statistical sections of protocols, including sample size calculations
  • Develop statistical analysis plans
  • Develop and document analysis database structures (i.e. SAS analysis data set structures)
  • Develop SAS program requirements and specifications
  • SAS programming and program validation
  • Review and QC of statistical deliverables (tables, listings, figures, etc.)
  • Perform statistical analysis and report results
  • Consult on experimental design, statistical methods and approaches for the purpose of assessing safety and efficacy of drug products
  • Liaise with DM on statistical questions related to data issues, including coordination of data transfers from DM to Statistics
  • Participate in bid defense meetings and kick-off meetings
  • Train statisticians and SAS programmers
  • Prepare and deliver presentations at investigators' meetings
  • Address audits findings/recommendations, and follow-up on and resolution of audit findings
Qualifications
  • MSc in Statistics or equivalent
  • Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research
  • Ability to apply a range of advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information
  • Ability to consult with clinical investigators, interpret research requirements, and determine statistical analysis strategies
  • Expert knowledge and understanding of the SAS programming
  • Expert knowledge and understanding of CDISC ADaM standard
  • Knowledge of relevant regulations and guidelines (e.g. FDA, EMA, ICH)
  • Ability to work in English 

Additional Information

Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.