<p><b>What role you will play in team:</b> You will support clinical trials by conducting statistical analysis and reporting.</p><p><b>What you will do:</b> You will plan, analyze, and interpret data from clinical trials, contributing to regulatory submissions.</p><p><b>Key responsibility:</b><ul><li>Plan and conduct statistical analysis of clinical trial data.</li><li>Prepare statistical reports and presentations.</li><li>Contribute to regulatory submissions.</li><li>Collaborate with clinical researchers.</li><li>Maintain data integrity and quality.</li><li>Use statistical software for analysis (e.g., SAS, R).</li></ul></p><p><b>Required Qualification and Skills:</b><ul><li>Master's or PhD in biostatistics or a related field.</li><li>Proficiency in statistical software (e.g., SAS, R).</li><li>Experience in clinical trials.</li><li>Excellent communication skills.</li><li>Knowledge of regulatory guidelines.</li></ul></p><p><b>Benefits Included:</b><ul><li>Competitive salary and benefits.</li><li>Opportunities for professional development.</li><li>A challenging and rewarding work environment.</li><li>Health Insurance</li><li>Retirement plan</li></ul></p><p><b>A Day in the Life:</b> You will spend your day analyzing data from clinical trials, preparing reports, and collaborating with other researchers.  You will contribute significantly to the development of new medicines.</p>