Website Alsinova
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:
- 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 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.
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.
- Fluency in written and spoken English.
- 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.
Alsinova
Alsinova is setting new standards for CROs by integrating multidisciplinary expertise with advanced technology. Alsinova offers a complete CRO solution, providing innovative, customised solutions in various life science segments: pharmaceuticals, biotechnology, medical devices, cosmetics, agri-food, veterinary and healthcare institutions.
Alsinova is the subsidiary of the Astek Group, a global player in engineering and technology consulting. Since its creation, the Group has based its development on a strong culture of entrepreneurship and innovation, and on the support and skills development of its 10.000 employees who are committed every day to promoting combination of digital technologies and complex systems engineering.
Join a Group rapidly developing in France and around the world, with a turnover of 705 M€ in 2024.
More on the Group on our websites https://alsinova.com and https://astek.net.
Astek is committed to the employment of people with disabilities.
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.