BioStatistician & Clinical statistician Programmer - Montréal, Canada (F/M) - Montreal - ALSINOVA CRO

    ALSINOVA CRO
    ALSINOVA CRO Montreal

    1 week ago

    Description

    Join to apply for the BioStatistician & Clinical statistician Programmer - Montréal, Canada (F/M) role at ALSINOVA CRO

    Role Overview


    Alsinova is seeking a Clinical Statistician Programmer in Oncology to provide study‑level statistical expertise in collaboration with the statistical team.

    Responsibilities

    • Program clinical datasets for regulatory submissions.
    • Write and execute SAS programs for data analysis and reporting.
    • Perform statistical analysis (normalization, linear and non‑linear regression, hypothesis testing) for biological assay data.
    • Analyze, integrate and report clinical trial data to produce quality and timely deliverables.
    • Support clinical studies by generating derived analysis data sets, tables, listings and figures, including quality control of those documents.
    • Participate in operations meetings and address issues that may influence statistical programming and data management.
    • Coordinate programming activities for the client.
    • Develop and validate study‑specific and cross‑project macros.
    • Validate statistical analysis and compile into statistical reports with interactive graphical outputs.
    • Contribute to standard processes (review SOPs, guidelines, define new processes).

    Qualifications

    • University level degree in Sciences, Engineering or Mathematics with a graduate degree in Biostatistics or equivalent background.
    • Minimum of 2 years of experience in clinical statistical programming or equivalent experience.
    • Good understanding of applied statistical principles in the design and analysis of clinical studies.
    • Experience in providing submission‑related study support.
    • Experience in statistical or clinical trial methodology research and presentations on statistical methods, clinical trial design and analysis in observational studies.
    • Extremely proficient in SAS programming (knowledge of other statistical software is an asset).
    • CDISC knowledge is an asset.
    • Experienced with internal SOPs and regulatory guidelines.
    • Knowledge of ICH Good Clinical Practices.
    • Reactive, team player, good communicator, collaborative attitude.
    • Ability to work with minimal supervision.
    • Strong attention to detail, comfortable managing multiple projects.
    • Ability to liaise theory with practical translation and share knowledge within multidisciplinary teams.
    • Fluency in written and spoken English.
    • Must be Canadian or have a work permit.

    Benefits

    • Experience accelerator: every assignment is an opportunity to progress.
    • Access to a multitude of technically exciting projects for clients and internally.
    • Individualized, local support for a tailored career path.
    • Continuous learning via internal training academy.
    • Friendly and inclusive work environment, supported by #TopEmployer2025 certified HR practices.

    Location: Montreal, Quebec, Canada | Salary: $90,000.00–$120,000.00 | Employment type: Full‑time | Seniority level: Entry level


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