<p><b>What role you will play in team:</b> You will be an integral part of our biostatistics team, applying statistical methods to analyze clinical trial data and support drug development. You will collaborate closely with other scientists and researchers.</p><p><b>What you will do:</b> You will design and conduct statistical analyses, prepare reports, and present findings to regulatory agencies and stakeholders. You will contribute to the design of clinical trials and provide statistical expertise.</p><p><b>Key responsibility:</b><ul><li>Design and conduct statistical analyses of clinical trial data.</li><li>Prepare statistical reports and presentations.</li><li>Collaborate with other scientists and researchers.</li><li>Provide statistical expertise in the design of clinical trials.</li><li>Interact with regulatory agencies.</li><li>Stay up-to-date on the latest advancements in biostatistics.</li></ul></p><p><b>Required Qualification and Skills:</b><ul><li>Master's or PhD in biostatistics or a related field.</li><li>2-4 years of experience in biostatistics.</li><li>Proficiency in statistical software (e.g., SAS, R).</li><li>Strong understanding of statistical methodology.</li><li>Experience with clinical trial data.</li><li>Excellent communication and presentation skills.</li></ul></p><p><b>Benefits Included:</b><ul><li>Competitive salary and benefits package.</li><li>Opportunities for professional development.</li><li>Work on impactful projects in the pharmaceutical industry.</li><li>Collaborative and supportive work environment.</li><li>Health insurance and other employee benefits.</li></ul></p><p><b>A Day in the Life:</b> A day involves analyzing clinical trial data, developing reports, participating in team meetings, and collaborating with other scientists. You'll be applying your statistical expertise to help develop life-saving medications.</p>