<p><strong>What role you will play in team:</strong> Collaborate with clinical research teams to design and analyze clinical trials for new pharmaceutical products.</p><p><strong>What you will do:</strong> Provide statistical support throughout the drug development process, ensuring high-quality data analysis.</p><p><strong>Key responsibility:</strong><ul><li>Design statistical analysis plans for clinical trials.</li><li>Analyze clinical trial data using appropriate statistical methods.</li><li>Prepare statistical reports and presentations for regulatory submissions.</li><li>Collaborate with clinical researchers and other stakeholders.</li><li>Maintain high standards of data quality and integrity.</li><li>Stay abreast of the latest advancements in biostatistics and clinical trial methodology.</li></ul></p><p><strong>Required Qualification and Skills:</strong><ul><li>Master's or PhD in Biostatistics or a related field.</li><li>2+ years of experience in biostatistics or a related role in the pharmaceutical industry.</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 collaboration skills.</li></ul></p><p><strong>Benefits Included:</strong><ul><li>Competitive salary and benefits package.</li><li>Opportunities for professional development.</li><li>Meaningful work contributing to the advancement of medicine.</li><li>Collaborative and supportive work environment.</li></ul></p><p><strong>A Day in the Life:</strong> Your day will involve designing statistical analyses, analyzing data from clinical trials, collaborating with scientists and preparing reports.</p>