<p><strong>What role you will play in team:</strong>  You will be an integral part of our clinical development team, providing statistical expertise to support the design and analysis of clinical trials.</p><p><strong>What you will do:</strong> You'll design study protocols, analyze clinical trial data, and write statistical reports to support regulatory submissions.</p><p><strong>Key responsibility:</strong><ul><li>Design and conduct statistical analyses of clinical trial data.</li><li>Develop statistical methods and models.</li><li>Prepare statistical reports and presentations for regulatory submissions.</li><li>Collaborate with clinical researchers and other stakeholders.</li><li>Ensure compliance with regulatory requirements.</li></ul></p><p><strong>Required Qualification and Skills:</strong><ul><li>Master's or PhD in Biostatistics, Statistics, or a related field.</li><li>Experience with statistical software packages (SAS, R).</li><li>Experience in clinical trial design and analysis.</li><li>Strong analytical and problem-solving skills.</li><li>Excellent communication and writing skills.</li></ul></p><p><strong>Benefits Included:</strong><ul><li>Competitive salary and benefits.</li><li>Opportunities for professional development.</li><li>Meaningful work in a life science setting.</li><li>Hybrid work option.</li></ul></p><p><strong>A Day in the Life:</strong> You will likely spend your day analyzing clinical trial data, developing statistical models, writing reports, collaborating with other team members, and ensuring compliance with regulatory requirements.</p>