Statistical Programmer

Statistical Programmer

Clinical Statistical Programmer - Biotech & Contract Research Organization (CRO)

An internationally recognized Contract Research Organization (CRO) that collaborates with leading pharmaceutical and biotechnology companies to accelerate the development of innovative treatments.

For over 35 years, this company has provided a comprehensive range of services covering the entire drug development lifecycle, including preclinical research, Phase I to IV clinical trials, bioanalysis, biomarkers, biostatistics, and clinical data management.

Through its scientific expertise, state-of-the-art facilities, and global presence, the company is recognized for the quality of its research and its key role in advancing new therapies that help improve the lives of patients around the world.

What sets this organization apart is its ability to combine the scientific excellence of a global leader with the agility and close-knit culture of a human-sized company. Employees work in a collaborative environment where innovation, scientific rigor, and professional development are at the heart of the company’s culture.

Joining this organization means contributing to internationally recognized research projects, collaborating with passionate experts, and playing a direct role in advancing healthcare solutions and the treatments of tomorrow.

As part of its continued growth, the company is currently seeking a Clinical Statistical Programmer (Statistical Programmer) to join its team.

Title : Clinical Statistical Programmer

Location : Montreal, 100% remote

Work model: 100% remote

Type of position: Full time, permanent

Salary: Open to discussion + Competitive group insurance (60% employer-paid)+ RRSP matching (up to 3%)+ 7 paid personal/sick days per year +3-4 weeks of vacation

The position is open to 100% remote candidates.

Reporting to the Programming Manager, you will be fully integrated into the team as a Clinical Statistical Programmer / SAS Programmer.

Your main responsibilities will include:

• Programming statistical databases in SAS using the CDISC standard.

• Programming statistical tables, figures, listings (TFLs), and statistical analyses using SAS.

• Creating regulatory submission packages, including Define.xml.

• Participating in software development using R and SAS.

Ideal candidate profile:

The ideal candidate will have:

• A degree in Data Science or a related field.

• Strong proficiency with SAS (version 9.4 and SAS Enterprise Guide).

• Knowledge of R, HTML/CSS/JavaScript, and PL/SQL.

• Knowledge of clinical trials and CDISC standards.

• Strong written English skills and French speaking

A previous experience in the pharmaceutical industry or at a Contract Research Organization (CRO) in a similar role is required.

What you will bring to this company:

• Strong attention to detail and adaptability.

• Energy and enthusiasm.

• A proactive mindset.

• The ability to organize and manage multiple projects simultaneously.