Statistical Programmer

Job summary

Program statistical databases, tables, figures, listings, and analyses in SAS using CDISC standards. Create regulatory submission packages, including Define.xml, and participate in software development using R and SAS.

Job details

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.

What you’ll do

Program statistical databases, tables, figures, listings, and analyses in SAS using CDISC standards. Create regulatory submission packages, including Define.xml, and participate in software development using R and SAS.

Requirements

A degree in Data Science or a related field, strong proficiency in SAS 9.4 and SAS Enterprise Guide, and knowledge of R, HTML/CSS/JavaScript, PL/SQL, clinical trials, and CDISC standards are sought. Previous experience in a similar pharmaceutical or CRO role is required, along with strong written English, French speaking ability, attention to detail, adaptability, and the ability to manage multiple projects.

Benefits

• Group Insurance • RRSP Matching • Paid Personal and Sick Days • Paid Vacation

Listed skills

• HTML · Preferred
• CSS · Preferred
• Attention to detail · Preferred
• JavaScript · Preferred
• Project management · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• SAS
• SAS Enterprise Guide
• R
• CDISC Standards
• Clinical Trials
• Statistical Programming
• TFL Programming
• Regulatory Submission Packages
• Define.xml
• HTML
• CSS
• JavaScript
• PL/SQL
• Attention to Detail
• Project Management
• Written English

Job areas

• Data & Analytics
• Science & Research
• Healthcare
• Technology