Statistician

Alimentiv; London; Remote; CAD 76,000 - 127,000; Full time

Job summary

An established industry player is seeking a Statistician to join their dynamic team. This role involves applying biostatistical methods to support clinical trials, ensuring compliance with regulatory standards while guiding project teams. You will play a crucial role in statistical planning, data management, and analysis, contributing to impactful research outcomes. With a focus on collaboration and expertise, this position offers the opportunity to work in a home-based environment, making a significant contribution to the pharmaceutical manufacturing sector. If you are passionate about statistics and eager to support innovative research, this is the perfect opportunity for you.

Qualifications

• 1-3 years of experience in biostatistics or related field.
• Strong understanding of statistical methods and regulatory standards.

Responsibilities

• Conduct statistical analyses and prepare reports for clinical trials.
• Collaborate on translating trial results into publishable findings.

Skills

Biostatistics

Statistical Analysis

Data Management

Regulatory Compliance

Education

Bachelor's Degree

Master's Degree

Tools

Statistical Software Packages

Job description

Join to apply for the Statistician role at Alimentiv.

The role involves 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. The statistician acts as a subject matter expert, providing statistical support to project teams, quality/study auditors, and external stakeholders. Additionally, the role includes contributing to the development, publishing, and reporting of project data, and promoting Alimentiv as a global research organization.

Key Responsibilities:

• Carry out statistical analyses and guide programmers, using standard software packages to interpret results within a biomedical framework, preparing data for reports and research papers that meet regulatory standards.
• Collaborate with the Director of Academic Research to translate trial technologies and findings into publishable scientific results.
• Provide statistical expertise throughout the project lifecycle, including study protocols, data interpretation, and publication of results.
• Work with data management to ensure data collection aligns with project protocols.
• Prepare statistical analysis plans and oversee data collection, management, and analysis, translating scientific questions into hypotheses.
• Assist 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 a professional designation, plus 1-3 years of related experience.

Working Conditions:

• Home-based.

Salary range: $76,000 - $127,000 per year + bonus.

Additional Details:

• Seniority level: Entry level.
• Employment type: Full-time.
• Job function: Research, Analyst, and Information Technology.
• Industry: Pharmaceutical Manufacturing.