<p><b>What role you will play in team:</b> Provide statistical expertise to support clinical trials and drug development programs.</p><p><b>What you will do:</b> Design study protocols, analyze clinical trial data, and prepare reports for regulatory submissions.</p><p><b>Key responsibility:</b><ul><li>Design study protocols and statistical analysis plans for clinical trials.</li><li>Analyze clinical trial data using appropriate statistical methods.</li><li>Prepare statistical reports for regulatory submissions.</li><li>Collaborate with clinicians and other scientists.</li><li>Maintain up-to-date knowledge of regulatory requirements.</li><li>Present findings at internal and external meetings.</li></ul></p><p><b>Required Qualification and Skills:</b><ul><li>Master's or PhD in Biostatistics or a related field.</li><li>1-2 years of experience in biostatistics or a related field.</li><li>Proficiency in statistical software (e.g., SAS, R).</li><li>Strong understanding of clinical trial design and methodology.</li><li>Excellent communication and report-writing skills.</li></ul></p><p><b>Benefits Included:</b><ul><li>Competitive salary and benefits package.</li><li>Opportunity to contribute to the development of life-saving medicines.</li><li>Collaborative and supportive work environment.</li><li>Professional development opportunities.</li></ul></p><p><b>A Day in the Life:</b>  Your day may involve data analysis, report writing, collaboration with clinical teams, and participation in project meetings.</p>