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BioStatistician & Clinical statistician Programmer F/M
Job Description & How to Apply Below
Join to apply for the Bio Statistician & Clinical statistician Programmer - Montréal, Canada (F/M) role at ALSINOVA CRO
Role OverviewAlsinova 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).
- 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.
- 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 #Top Employer
2025 certified HR practices.
Location:
Montreal, Quebec, Canada | Salary: $90,000.00–$ |
Employment type:
Full‑time | Seniority level:
Entry level
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