<p><b>What role you will play in team:</b> You will provide statistical support for clinical trials. </p><p><b>What you will do:</b> You will design studies, analyze data, and prepare reports for regulatory submissions. </p><p><b>Key responsibility:</b><ul><li>Design and conduct statistical analyses for clinical trials.</li><li>Prepare statistical reports for regulatory submissions.</li><li>Collaborate with clinical researchers and other statisticians.</li><li>Develop and maintain statistical models.</li><li>Ensure the quality and integrity of statistical analyses.</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>Strong programming skills in R or SAS.</li><li>Experience with clinical trial data.</li><li>Knowledge of statistical methods used in clinical trials.</li><li>Excellent communication skills.</li></ul></p><p><b>Benefits Included:</b><ul><li>Competitive salary and benefits.</li><li>Opportunities for professional development.</li><li>Meaningful work contributing to global health.</li><li>Strong work life balance and flexible working options.</li></ul></p><p><b>A Day in the Life:</b> Involves statistical programming, data analysis, report writing and collaborating with other team members on clinical trial studies.</p>