<p><strong>What role you will play in team:</strong> Contribute to the design and analysis of clinical trials for new pharmaceuticals.</p><p><strong>What you will do:</strong> Analyze clinical trial data, prepare reports, and collaborate with other scientists.</p><p><strong>Key responsibility:</strong><ul><li>Design and conduct statistical analyses of clinical trial data.</li><li>Prepare statistical reports and presentations.</li><li>Collaborate with other biostatisticians, clinicians, and scientists.</li><li>Develop and maintain statistical models.</li><li>Ensure data integrity and quality.</li><li>Stay up-to-date with the latest statistical methodologies.</li></ul></p><p><strong>Required Qualification and Skills:</strong><ul><li>Master's or PhD degree in Biostatistics or Statistics.</li><li>1-2 years of experience in clinical trial analysis.</li><li>Proficiency in statistical software (e.g., SAS, R).</li><li>Knowledge of clinical trial design and methodology.</li><li>Excellent communication and presentation skills.</li></ul></p><p><strong>Benefits Included:</strong><ul><li>Competitive salary and benefits package.</li><li>Opportunities for professional development and growth.</li><li>Collaborative and supportive work environment.</li></ul></p><p><strong>A Day in the Life:</strong> A typical day involves data analysis, report writing, collaboration with colleagues, and project meetings.</p>