<p><strong>What role you will play in team:</strong> Support clinical trials by providing statistical expertise and analysis.</p><p><strong>What you will do:</strong> Design and conduct statistical analyses of clinical trial data.</p><p><strong>Key responsibility:</strong><ul><li>Design statistical analysis plans for clinical trials.</li><li>Conduct statistical analyses of clinical trial data.</li><li>Prepare statistical reports and presentations.</li><li>Collaborate with clinical research teams.</li><li>Ensure adherence to regulatory guidelines.</li><li>Stay up-to-date on statistical methods and regulatory requirements.</li></ul></p><p><strong>Required Qualification and Skills:</strong><ul><li>Master's or PhD in Biostatistics or related field.</li><li>Experience in clinical trials.</li><li>Proficiency in statistical software (e.g., SAS, R).</li><li>Excellent communication and collaboration skills.</li><li>Knowledge of regulatory guidelines.</li></ul></p><p><strong>Benefits Included:</strong><ul><li>Competitive salary and benefits.</li><li>Opportunity to work on important clinical trials.</li><li>Collaborative and supportive work environment.</li><li>Opportunities for professional development.</li></ul></p><p><strong>A Day in the Life:</strong>  A day involves analyzing data, preparing reports, and collaborating with other scientists.</p>