<p><b>What role you will play in team:</b> You will support clinical trials by designing experiments, analyzing data, and writing reports. Collaborate with scientists and clinicians to ensure data integrity and accuracy.</p><p><b>What you will do:</b>  Design statistical plans for clinical trials, analyze clinical trial data, and prepare reports for regulatory submissions.</p><p><b>Key responsibility:</b><ul><li>Design statistical 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 scientists and clinicians to ensure data integrity.</li><li>Stay up-to-date with the latest statistical methods and regulations.</li></ul></p><p><b>Required Qualification and Skills:</b><ul><li>Master's or PhD degree in biostatistics or a related field.</li><li>Experience with statistical software such as SAS or R.</li><li>Strong understanding of clinical trial design and methodology.</li><li>Excellent communication and writing skills.</li><li>Experience in the pharmaceutical industry is a plus.</li></ul></p><p><b>Benefits Included:</b><ul><li>Competitive salary and benefits package.</li><li>Opportunities for professional development.</li><li>Health insurance.</li><li>Retirement plan.</li><li>Paid time off.</li></ul></p><p><b>A Day in the Life:</b>  Your day will involve statistical programming, data analysis, report writing, and collaborating with cross-functional teams.</p>