Senior Statistician

Summary

Join Alimentiv as a Biostatistician to apply biostatistical methods in clinical trials and data management. You will be responsible for statistical planning, design, analysis, and reporting throughout the project lifecycle. Act as a subject matter expert, providing statistical support to project teams and stakeholders. Contribute to the development, publishing, and reporting of project data. Multiple positions are available. This is a home-based position with a salary range of $115,500 - $144,500 a year, plus bonus.

Requirements

A minimum of a Bachelor's or Master's degree and a professional designation + 1-3 years of related experience

Responsibilities

• Carry out statistical analyses and provide direction to programmers, using standard software packages to interpret and translate results within a statistical framework into biomedical terms and prepare statistical data results for inclusion in reports and research papers that meet trial, organizational and regulatory best practices, and standards
• Working in conjunction with the Director of Academic Research, convert and present new and novel biometrical trial technologies, processes and findings into publishable and promotable scientific processes and results
• Provide statistical expertise and guidance based on established methodologies throughout the project life cycle in the areas of study policies, protocols, implementation timelines and processes, data interpretation and publication of results
• Work with data management team to ensure data captured incorporates and corresponds to project protocols and requirements
• Prepare statistical analysis plan and oversee project data collection, management, and analysis with input from the project teams that incorporates the type of information collected, sample size, randomization procedures, table and listing shells, project statistical policies, protocols, and methodology to be used to appropriately translate scientific questions into statistical hypotheses
• Assist medical director(s) and/or technical writers by preparing statistical section of study report, publications and/or presentations ensuring statistical analyses adheres to trial, sponsor, organizational and regulatory requirements, and best practices

Preferred Qualifications

Experience working with clinical research data/within clinical research organization

Benefits

• $115,500 - $144,500 a year
• +bonus
• Home-based