Senior/Principal Statistical Programmer/Analyst Consultant

Senior/Principal Statistical Programmer/Analyst Consultant Canada

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds...

ClinChoice is searching for a

Senior/Principal Statistical Programmer Consultant

to join one of our clients.

The

Senior Statistical Programmer

will serve as a senior technical expert responsible for end-to-end programming deliverables, study leadership, and oversight of internal teams and external vendors. This role requires advanced expertise in

SAS , familiarity with

R , deep knowledge of

CDISC standards , and strong experience working on oncology studies and regulatory submissions.

Key Responsibilities Technical Leadership

Lead programming activities for oncology clinical trials across multiple studies.

Develop, validate, and maintain

SDTM and ADaM datasets

following CDISC guidelines.

Oversee production of

Tables, Listings, and Figures (TLFs)

for study reporting and submissions.

Provide SAS programming expertise to support complex data derivations and analyses.

Review and ensure traceability, consistency, and quality of all programming deliverables.

Project & Study Management

Act as programming lead for assigned studies, managing timelines and deliverables.

Work closely with Biostatistics, Data Management, Medical Writing, and Regulatory Affairs.

Coordinate with CROs and external vendors, ensuring compliance, quality, and adherence to client programming standards.

Support integrated analyses including

ISS/ISE .

Regulatory & Submission Support

Prepare submission-ready programming outputs and documentation, including define.xml, annotated CRFs, and reviewer guides.

Ensure all programming meets regulatory requirements (FDA, EMA, PMDA).

Contribute to responses for regulatory queries and data requests.

Required Qualifications

Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field.

6–10+ years of statistical programming experience in pharma/biotech or CRO.

Expert-level proficiency in

SAS .

Strong understanding of

CDISC SDTM and ADaM

standards.

Significant experience supporting

oncology clinical trials

(hematologic or solid tumors).

Experience supporting

regulatory submissions

and preparing submission-ready outputs.

Excellent communication skills and ability to collaborate cross-functionally.

Vacancy: This posting is for an existing vacancy.

Open Date: 02/27/2026

Close Date: 03/27/2026

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.

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.

$60 - $80 CAD

#J-18808-Ljbffr