<p><b>What role you will play in team:</b> You will be an integral part of a team conducting statistical analyses to support the development and regulatory submissions of pharmaceutical products.</p><p><b>What you will do:</b> You'll design and conduct statistical analyses, interpret results, prepare reports, and present findings to internal and external stakeholders.</p><p><b>Key responsibility:</b><ul><li>Design and conduct statistical analyses of clinical trial data.</li><li>Prepare statistical analysis plans and reports according to regulatory guidelines.</li><li>Interpret statistical results and provide meaningful conclusions.</li><li>Collaborate with clinical scientists and other members of the research team.</li><li>Present findings to internal and external stakeholders.</li><li>Ensure data quality and integrity.</li></ul></p><p><b>Required Qualification and Skills:</b><ul><li>Master's or PhD degree in Biostatistics or a related field.</li><li>Experience with statistical software such as SAS, R, or SPSS.</li><li>Knowledge of clinical trial design and methodology.</li><li>Excellent communication and presentation skills.</li><li>Strong understanding of regulatory requirements.</li></ul></p><p><b>Benefits Included:</b><ul><li>Competitive salary and comprehensive benefits package.</li><li>Opportunities for professional growth and development within a leading pharmaceutical company.</li><li>Collaborative and supportive work environment.</li><li>Contribution to the development of life-saving medications.</li></ul></p><p><b>A Day in the Life:</b> A typical day could involve data analysis, report writing, meetings with clinical scientists, and preparation for regulatory submissions.</p>