Statistical Programmer II - Quebec

When our values align, there's no limit to what we can achieve. ·   · At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by someth ...

Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Statistical Programmer II (R Focus) – Canada (Remote)

Join Parexel and make a meaningful impact on global health.

Parexel is seeking an R-focused Statistical Programmer II to join our team in Canada, fully dedicated to a single sponsor. This is a 100% remote, full-time opportunity offering the chance to contribute to high‑visibility clinical trials, grow your expertise, and enjoy long-term career stability.

In this role, you will provide technical programming expertise to support the analysis and reporting of clinical study data. Working with minimal supervision, you will handle a variety of programming activities and may also serve as a Statistical Programming Lead (or contribute to that role) for smaller, non‑complex projects.

At Parexel FSP, you'll experience:

• Exceptional long-term career security
• Opportunities to work with leading global biopharma and biotech organizations
• An extensive pipeline of impactful clinical research projects
• A supportive environment that values work–life balance and professional growth

Expect inspiring scientific challenges with room to enjoy life outside of work.

Key Responsibilities

• Assist in coordinating project start-up activities, including global program creation, tracking spreadsheets, and required documentation.
• Continuously check your own work to ensure first-time quality.
• Apply efficient programming techniques to produce derived datasets (e.g., SDTM, ADaM), tables, figures, and data listings of any complexity; perform QC for low–medium complexity datasets, tables, figures, and listings.
• Assist in producing and QC'ing derived dataset specifications, process-supporting documents, and submission documentation.
• Maintain and expand knowledge of both local and international regulatory requirements within clinical research.
• Build expertise in SAS and gain an understanding of processes within other Parexel functional areas.
• Provide relevant training and mentorship to colleagues and project teams.
• Maintain complete and accurate study documentation according to SOPs/Guidelines to ensure traceability and regulatory compliance.
• Ensure compliance with SOPs/Guidelines, ICH-GCP, and other applicable regulations (including 21 CFR Part 11); participate in internal/external audits and regulatory inspections as needed.
• Proactively contribute to process and quality improvement initiatives.
• Understand regulatory expectations related to industry technical standards (e.g., CDISC, 21 CFR Part 11, electronic submissions).

Role-Specific Requirements

• Bachelor's degree in statistics, biostatistics, mathematics, computer science, or life sciences.
• Excellent analytical skills.
• Intermediate proficiency in the R programming language.
• Knowledge of programming and reporting processes.
• Understanding of SOPs/Guidelines, ICH-GCP, and applicable regulations such as 21 CFR Part 11.
• Ability to learn new systems and work effectively in an evolving technical environment.
• Strong ability to manage competing priorities and adapt to change.
• Proven success working as part of a global team.
• Effective time management to meet daily metrics and team objectives.
• Business and operational skills including customer focus, commitment to quality, and problem‑solving.
• Strong understanding of CDISC standards.
• Knowledge of statistical terminology, clinical tests, and protocol designs.
• Excellent attention to detail with a commitment to quality.
• Strong written and verbal English communication skills.

Why Parexel?

At Parexel, we care deeply about our people — your expertise, your growth, and your passion are central to our success. We offer an open and collaborative work environment where you are empowered to thrive and advance your long-term career.

You'll also have opportunities to expand your responsibilities within your role or build your capabilities across related departments.

Parexel supports clinical studies across the full range of therapeutic areas and has longstanding partnerships with a broad client base. We have contributed to trials for most of today's top 50 best‑selling drugs, while also supporting innovative niche therapies essential to patient well‑being.

As a Statistical Programmer II, you'll be an influential contributor within a dedicated and highly collaborative global team.