Statistician

Alimentiv 2; Boston (MA); On-site; USD 80,000 - 120,000; Full time

Job summary

Alimentiv 2 is seeking a biostatistician based in Boston, Massachusetts, to support clinical trials through the application of biostatistical methods. The successful candidate will be responsible for statistical planning, design, analysis, and reporting throughout project life cycles.

Key responsibilities include preparing statistical analysis plans, providing expertise to project teams, and ensuring compliance with regulatory standards. The ideal candidate will contribute to the development of publishable research results and maintain strict adherence to best practices.

Qualifications

• Expertise in biostatistical methods and clinical trials.
• Ability to prepare statistical result reports and publications.
• Strong collaboration and communication skills with project teams.

Responsibilities

• Responsible for application of biostatistical methods to clinical trials.
• Prepare statistical analysis plans and oversee data collection.
• Provide statistical guidance throughout the project life cycle.
• Convert trial technologies into publishable scientific results.
• Assist in preparing statistical sections of reports and presentations.

Job description

Responsibilities

Responsible for the application of biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and reporting throughout the project life cycle in accordance with project, organizational and regulatory standards. Act as subject matter expert, providing statistical support to project teams, quality/study auditors, and external stakeholders. Participate in the promotion of Alimentiv as a global research organization, by contributing to the development, publishing, and reporting of project data.

• 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.