BioStatistician & Clinical statistician Programmer

Keyrus Life Science North America; Canada; On-site; CAD 40,000 - 70,000; Part time

Job summary

A leading international CRO, Keyrus Life Science North America is seeking a part-time Clinical Statistician Programmer to provide statistical expertise in clinical development. The candidate will be responsible for analyzing data for submissions, ensuring quality deliverables, and collaborating within interdisciplinary teams. This role offers a comprehensive salary package with attractive benefits, and an immediate start is available.

Benefits

Pension plan

Health insurance

Training and development programs

Qualifications

• Minimum 2 years of experience in clinical statistical programming.
• Proficient in SAS programming and knowledge of CDISC is a plus.
• Fluent in English.

Responsibilities

• Prepare clinical datasets for regulatory submissions.
• Write and execute SAS programs for data analysis.
• Analyze and report clinical trial data.

Skills

Applied statistical principles

SAS programming

Statistical analysis

Team collaboration

Attention to detail

Education

University degree in Sciences, Engineering, or Mathematics

Graduate degree in Biostatistics or equivalent

Job description

Clinical Statistician Programmer/Oncology - URGENT 20 hours/week (Part Time)

Role

The clinical statistical programmer will be responsible for providing study-level statistical expertise in collaboration with other team members.

The clinical statistical programmer will also be responsible for providing statistical programming expertise to support clinical development and medical teams.

Profile :

• You must be Canadian (or have a Canadian work permit).
• You have a good understanding of applied statistical principles in the design and analysis of clinical studies.
• You hold a university degree in Sciences, Engineering, or Mathematics, with a graduate degree in Biostatistics or an equivalent educational background.
• You have a minimum of 2 years of experience in clinical statistical programming or equivalent experience.
• 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 can manage multiple projects simultaneously.
• You can relate theory to practical applications.
• You have the ability to share knowledge and collaborate within multidisciplinary teams.
• You have experience in providing submission-related study support.
• You have experience in statistical or clinical trial methodology research and presentations on statistical methods, clinical trial design, and analysis in 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 an asset.
• Fluency in written and spoken English.
• You are accustomed to complying with internal Standard Operating Procedures and regulatory guidelines.
• Knowledge of ICH Good Clinical Practices.

Key Responsibilities:

• Preparing clinical datasets for regulatory submissions.
• Writing and executing SAS programs for data analysis and reporting.
• Performing statistical analyses such as normalization, linear regression, non-linear regression, and hypothesis testing for biological assay data in drug discovery.
• Analyzing, integrating, and reporting clinical trial data to produce quality, timely deliverables.
• Providing statistical programming support for clinical studies, including quality control of analysis data sets, tables, listings, and figures.
• Participating in operational meetings and addressing issues affecting programming and data management.
• Coordinating programming activities for the client.
• Developing and validating study-specific and cross-project macros.
• Performing and validating statistical analyses and compiling reports with graphical outputs.
• Contributing to standard processes and SOP reviews.

Initial contract length: 20 hours/week (potentially increasing), 1 year with renewal.

Start date: as soon as possible.

What we offer

At Keyrus, we welcome employees with varied integration programs in a dynamic, international environment with enthusiastic colleagues.

We invest in training (technical and non-technical) to support your growth. You will receive a comprehensive salary package with attractive benefits (pension, health insurance, etc.) based on your experience.

Who we are

Keyrus Life Science is an international CRO and consulting provider known for transparency, integrity, and excellence. Our human approach and high-caliber staff differentiate us in clinical research.

We are committed to delivering high-quality services across all stages of drug development, including project management, clinical operations, pharmacovigilance, regulatory affairs, data management, biostatistics, medical review, and more.