• Programming deliveries through preparation of clinical datasets for regulatory submissions.
• Writing and executing SAS programs for data analysis and reporting.
• Performing statistical analysis such as normalization, linear regression, non-linear regression and hypothesis testing for different biological assay data with various plates formats in drug discovery process.
• Responsible for statistical programming activities. That includes, but is not limited to: analyzing, integrating and reporting of clinical trial data in order to produce quality and timely deliverables.
• Responsible for statistical programming activities in order to produce adequate and timely deliverables.
• Provide statistical programming support for clinical studies through generation of derived analysis data sets, tables, listings, and figures, including quality control of those documents.
• Participating in operations meetings and address issues that may influence statistical programming and data management.
• Coordinating programming activities for the client
• Development/validation of study specific and cross project macros
• Performing/validating statistical analysis and compiling those into statistical reports including interactive graphical outputs.
• Input in standard processes (review of Standard Operating Procedures, guidelines, definition of new processes needed)

You

• You hold a university level degree in Sciences, Engineering or Mathematics with a graduate degree in Biostatistics or equivalent educational background.
• You have a minimum of 2 years of experience in clinical statistical programming or equivalent experience.
• You have a good understanding of applied statistical principles in the design and analysis clinical studies.
• You have experience in providing submission-related study support.
• You carry experience in statistical or clinical trial methodology research and presentations on statistical methods, clinical trial design, and analysis in either observational studies.
• You are extremely proficient in SAS programming (knowledge of other statistical software is an asset).
• If you have CDISC knowledge, it will be considered as a an asset.
• You are used to comply with internal Standard Operating Procedures and regulatory guidelines.
• Knowledge of ICH Good Clinical Practices.
• You are very reactive.
• You are a team player, good communicator and have a collaborative attitude.
• You have the ability to work with minimal supervision.
• You have strong attention to detail and are comfortable managing multiple projects at once.
• You have the ability to liaise theory with the practical translations.
• You have the ability to share knowledge and interact within multidisciplinary teams.
• Fluency in written and spoken English.
• You must be Canadian (or have a Canadian work permit).

Our Benefits Joining Astek means choosing:

• an experience accelerator, where every assignment is an opportunity to progress
• access to a multitude of technically exciting projects for our clients as well as internally
• individualized, local support for a tailored career path
• continuous learning, thanks to our internal training academy
• a friendly and inclusive work environment, supported by #TopEmployer2025 certified HR practices Let's move forward.

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