Senior Statistician

Natural Factors; London; Remote; CAD 115,000 - 145,000; Full time

Job summary

An established industry player is seeking a skilled biostatistician to apply statistical methods in clinical trials and data management. This role involves collaborating with project teams to ensure compliance with regulatory standards while contributing to innovative research findings. The position offers flexibility with a home-based working environment, making it ideal for professionals looking to balance work and personal commitments. If you are passionate about biostatistics and eager to make an impact in clinical research, this opportunity could be your next career move.

Qualifications

• 1-3 years of experience in biostatistics or clinical research.
• Professional designation preferred.

Responsibilities

• Apply biostatistical methods to support clinical trials and data management.
• Develop statistical analysis plans and oversee data collection.

Skills

Biostatistics

Statistical Analysis

Data Management

Clinical Research

Education

Bachelor's Degree

Master's Degree

Job description

Responsible for applying biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and reporting throughout the project lifecycle in accordance with project, organizational, and regulatory standards. Acts as a subject matter expert, providing statistical support to project teams, quality/study auditors, and external stakeholders. Contributes to promoting Alimentiv as a global research organization by developing, publishing, and reporting project data. Multiple positions are currently available.

Analysis Services

• Carry out statistical analyses and guide programmers, using standard software packages to interpret results within a biomedical framework and prepare data for reports and research papers that meet trial, organizational, and regulatory standards.

Academic Research Support

• Collaborate with the Director of Academic Research to convert and present innovative biometrical trial technologies, processes, and findings into publishable scientific results.

Project Support

• Provide statistical expertise throughout the project lifecycle, advising on study policies, protocols, timelines, data interpretation, and publication of results.
• Coordinate with the data management team to ensure data collection aligns with project protocols and requirements.

Statistical Analysis/Data Collection Planning

• Develop statistical analysis plans and oversee data collection, management, and analysis, ensuring appropriate translation of scientific questions into hypotheses.

Study Report Support

• Assist medical directors and technical writers in preparing statistical sections of study reports, publications, and presentations, ensuring compliance with standards and best practices.

Qualifications

• Bachelor's or Master's degree with 1-3 years of related experience; professional designation preferred.
• Experience with clinical research data or within a clinical research organization is a plus.

Working Conditions

• Home-based position.

Salary range: $115,500 - $144,500 per year plus bonus. Accommodations available upon request.