<p><b>What role you will play in team:</b> You will play a vital role in clinical trials by designing, analyzing, and interpreting clinical trial data.  Collaborate closely with medical and scientific teams.</p><p><b>What you will do:</b> Conduct statistical analysis, prepare reports, and present findings on clinical trials data, focusing on drug efficacy and safety.</p><p><b>Key responsibility:</b><ul><li>Design and conduct statistical analyses of clinical trial data.</li><li>Prepare statistical reports and presentations for regulatory submissions.</li><li>Collaborate with medical and scientific teams to interpret results.</li><li>Ensure compliance with regulatory guidelines.</li><li>Contribute to the development of statistical analysis plans.</li><li>Present findings clearly and concisely to both technical and non-technical audiences.</li></ul></p><p><b>Required Qualification and Skills:</b><ul><li>Master's or PhD in Biostatistics or a related field.</li><li>Experience with statistical software such as SAS or R.</li><li>Strong understanding of clinical trial methodology.</li><li>Excellent communication and presentation skills.</li><li>Knowledge of regulatory guidelines for clinical trials is a plus.</li></ul></p><p><b>Benefits Included:</b><ul><li>Competitive salary and benefits package.</li><li>Opportunities for professional development and advancement.</li><li>Meaningful work contributing to the development of life-saving medicines.</li></ul></p><p><b>A Day in the Life:</b>  Involves data analysis using statistical software, report writing, and collaborating with medical and scientific teams to discuss results.</p>