Statistical and Research Analyst

This opening is for our Medical Research & Development team.
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. Lead and develop a group of statisticians and SAS Programmers.
Analysis Services
~ 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.

Academic and Project Research Support
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.
Statistical Analysis/Data Collection Planning and Study Report Support
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.
Assign/schedule studies and tasks to functional unit to ensure project needs are met.
Responsible for performance management (staff evaluation performance improvement and lost time management) of direct reports.
Provide direction and support to project financial coordinators and promote team development by providing coaching mentoring and training.
Develop and deliver ongoing training on document user systems document naming and department Quality System processes to peers and stakeholders including new employee orientation.
The successful candidate should hold a minimum of an undergraduate degree with professional certifications and 4-6 years of professional experience. PhD with experience in research is a strong asset.
Experience in the industry or in an academic setting is preferred.
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Senior IC