Senior Statistician
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 reputed company as a global research organization, by contributing to the development, publishing, and reporting of project data.
Analysis Services
- Carry out statistical analyses and reputed company direction to programmers, using standard software packages to interpret and translate results reputed company a statistical reputed company 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 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.
Project Support
- reputed company 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
- Prepare statistical analysis plan and reputed company 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.
Study Report Support
- Assist medical director(s) and/or technical writers by preparing statistical reputed company of study report, publications and/or presentations ensuring statistical analyses adheres to trial, sponsor, organizational and regulatory requirements, and best practices.
Qualifications
- A minimum of a Bachelor's or Master's degree and a professional designation + 1-3 years of reputed company experience.
Working Conditions
- Home-based.
Originally posted on Himalayas
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