Alsinova provides end-to-end life science research services that combine medical expertise with AI-driven tools. As a non-clinical and clinical research company, Alsinova uses a Digital CRO approach, data science, automation, and machine learning to deliver RWE, regulatory affairs, and vigilance support. It operates across 26 countries with flexible collaboration models. Supported by AI and human experts, it tailors solutions for pharma, biotech, and medical device clients. The company targets global life science programs with scalable partnerships.
BioEquivalenceBiostatisticsClinical Data FabricClinical OperationsClinical Project ManagementClinical ResearchConsultingData ManagementData SciencesDecentralized Clinical TrialsDigital EnablementeHealthFSPLife SciencesMedical WritingPhase I to IVQuality AssuranceRegulatoryRWESafetyVigilancealsinova.com
ALSINOVA CRO
Alsinova provides end-to-end life science research services that combine medical expertise with AI-driven tools. As a non-clinical and clinical research company, Alsinova uses a Digital CRO approach, data science, automation, and machine learning to deliver RWE, regulatory affairs, and vigilance support. It operates across 26 countries with flexible collaboration models. Supported by AI and human experts, it tailors solutions for pharma, biotech, and medical device clients. The company targets global life science programs with scalable partnerships.
BioEquivalenceBiostatisticsClinical Data FabricClinical OperationsClinical Project ManagementClinical ResearchConsultingData ManagementData SciencesDecentralized Clinical TrialsDigital EnablementeHealthFSPLife SciencesMedical WritingPhase I to IVQuality AssuranceRegulatoryRWESafetyVigilancealsinova.com
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What we will accomplish together:
Alsinova is looking for a
Clinical Statistician programmer in Oncology
This position is fully dedicated to a client in an hybrid model ( 2 days in the office if located in Montreal area)
Your mission (should you decide to accept it):
The clinical statistical programmer will be responsible for providing study level statistical expertise hand to hand with the other statistical team member The clinical statistical programmer will also be responsible for Providing statistical programming expertise to the development, validation and supporting Clinical development and Medical team.
Your daily activities will be:
You:
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.
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 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).
