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Senior Statistical Programmer Analyst - Permanent Role_Canada
@ ClinChoice
Mississauga, Ontario
Overview
ClinChoice is hiring a Senior Statistical Programmer for its in-house team to lead statistical programming for clinical trials across pharmaceutical, biotech, medical device and consumer health clients. The role covers derived datasets, CDISC-compliant electronic submissions, oversight of CRO and vendor programming, and mentoring other programmers. It is a permanent, remote role with a base range of $80,000 to $95,000 CAD.
Responsibilities:
- Program and validate derived datasets, tables, figures and listings
- Lead CDISC-compliant electronic submission deliverables
- Oversee programming work from CROs and external vendors
- Contribute to CRF, DTS, SAP and SDTM/ADaM specification design and review
- Help develop standards, macros and utilities
Requirements summary:
- Degree in computer science, mathematics, engineering or related field
- 5+ years (BS) or 3+ years (MS) statistical programming in pharma
- Strong SAS and SAS macro language skills
- R programming in clinical trials
- Knowledge of industry standards and drug development
- Strong oral and written communication skills
Tools & skills
Source and dates
Employer career site / ATS feed · greenhouse
- Employer posting date
- 2026-09-29
- First seen by our source
- 2026-10-11
- Source record updated
- 2026-10-26
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Senior |
| Department | Data & analytics |
| Experience | 3+ years |
| Hours per week | 40 (estimated) |
| Work setting | Home |
| Position | Mostly sitting |
| Physical demands | physical low · computer high |
| Languages | English |
| Education | Bachelor’s degree (required), Master’s degree (preferred) |
| Fields of study | Computer Science, Mathematics, Engineering, Medical, Related discipline |
Summary and details written by AI from the posting; the employer’s posting is the authority.
ClinChoice
Saved company profile
Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.
The Standard of Excellence
Full company description
ClinChoice is a leading global full & functional service CRO, renowned for its exceptional product development and lifecycle management capabilities across the pharmaceutical, biotechnology, medical device, and consumer health sectors. With three decades of proven expertise and outstanding results, we excel in delivering top-tier services. Our deep regulatory expertise, clinical trial execution, and robust pharmacovigilance and biometrics capabilities position us as a trusted partner in global markets. ClinChoice proudly maintains a strong presence across the Americas, Europe, and Asia-Pacific, ensuring comprehensive support for our clients worldwide.
- LinkedIn followers
- 130,006
- People associated on LinkedIn
- 1,625
- Reported office locations
- 300 Welsh Road, Building 5, Suite 201, Horsham, Pennsylvania 19044, US
- Business categories
- Health Care
- Consulting
- Data Management
- Biotechnology
- Medical
- Pharmaceutical
- Other recorded names
- ClinChoice
- Specialties
- Full-Service CRO
- Clinical Development
- Post-Marketing & Real-World Evidence
- Quality and Compliance
- Technology
- Consulting
- FSP Solution
- Full-Service Solutions
- Pharma and Biotech
- Medical Device and Diagnostics
- Consumer Health
- and Project Management
- Profile identifies a recruitment agency
- No
- Reported total investment
- 212,000,000
Currency and observation date were not supplied; this is not a current valuation or a funding round.
ClinChoice is a leading global full & functional service CRO, renowned for its exceptional product development and lifecycle management capabilities across the pharmaceutical, biotechnology, medical device, and consumer health sectors. With three decades of proven expertise and outstanding results, we excel in delivering top-tier services. Our deep regulatory expertise, clinical trial execution, and robust…
| Field | Value |
|---|---|
| Industry | Pharmaceutical Manufacturing |
| Company size | 1,001-5,000 employees |
| Headquarters | Horsham, Pennsylvania |
| Organization type | Privately Held |
| Year founded | 1995 |
| Specialties | Full-Service CROClinical DevelopmentPost-Marketing & Real-World EvidenceQuality and ComplianceTechnologyConsultingFSP Solution Full-Service SolutionsPharma and BiotechMedical Device and Diagnostics |
| Open jobs on Jobsy | 7 |
| View page |
ClinChoice is a global full-service CRO committed to professional growth and a quality-driven “one-team” culture. We are seeking a Senior Statistical Programmer to join our in-house team and support projects across a diverse client portfolio, including pharmaceutical, biotechnology, medical device, and consumer health companies of varying sizes.
We are seeking a highly skilled Senior Statistical Programmer to lead statistical activities for clinical trials. This role requires hands-on statistical expertise, strong communication skills, and the ability to independently lead projects while collaborating closely with cross-functional teams.
Join our team: you can be part of making a difference in peoples' lives and experience a fulfilling and rewarding career!
Main Job Tasks
The Senior Statistical Programmer is a delivery-focused role responsible for leading and supporting aspects of the programming effort to deliver technical programming and information components of a project. The position requires strong technical skills, thorough knowledge of the industry, and demonstrated experience leading statistical programming activities and providing technical guidance to other programmers. The individual should be able to independently perform programming tasks, oversee programming deliverables, and effectively collaborate with cross-functional teams and external vendors.
Responsibilities
Programing for clinical trials:
Program and validate derived datasets, tables, figures, listings. Process data from the external sources.
Perform ad hoc exploratory analyses for publications and programming support other functions of Research and Development or other organizations.
Oversee programing work/deliverables from CROs.
Contribute to the design/implementation/review of Case Report Form, Data Transfer Specification, Statistical Analysis Plan, SDTM/ADaM Specification documents, Define packages.
Electronic submissions:
Program and validate CDISC compliant deliveries for the electronic submissions.
Support in the creation of supporting documentation for submissions.
Project Management:
Ensure programming deliverables are on time and of high quality.
Help managing internal contractors and external vendors.
Standards and Guidelines:
Participate in development of departmental working instructions and guidelines.
Help in creation of enhanced functions/macros and utilities.
Qualification & Experience
- Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline.
- BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry.
- Working knowledge of SAS and its various components.
- Knowledge of R programming in clinical trials
- Familiarity of the drug development process.
- Strong SAS and SAS Macro language skills.
- R programming skils in clinical trials
- Strong knowledge of industry standards.
- Ability to work on data integrations (ISS and ISE).
- Strong oral and written communication skills. Ability to communicate details of the analysis to other team members with less technical experience.
Open Date: 9/29/2026
Close Date: 11/23/2026
ClinChoice Canada Inc. is proud to be an equal opportunity employer, valuing and respecting diversity. We are committed to inclusive, barrier-free recruitment and selection processes. We will accommodate the needs of qualified applicants under the Human Rights Code and the Accessibility for Ontarians Disabilities Act, in all aspects of the hiring process, upon request by calling + 1 (647)724-5709 x 301.
We thank all applicants for their interest; however, only those being considered for an interview will be contacted. In accordance with Federal Personal Information Protection and Electronic Documents Act ("PIPEDA") , personal information is collected under the authority of the Act and will only be used for candidate selection.
#LI-TT1 #LI-Remote #senior #permanent
The base salary pay range represents the anticipated low and high range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.
Canada Pay Range
$80,000—$95,000 CAD
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