<p><strong>What role you will play in team:</strong> You will be a member of a team of biostatisticians supporting clinical trials and the development of new pharmaceutical products.</p><p><strong>What you will do:</strong> You'll design statistical analyses, analyze clinical trial data, and prepare reports for regulatory submissions.</p><p><strong>Key responsibility:</strong><ul><li>Design and conduct statistical analyses of clinical trial data.</li><li>Prepare statistical reports for regulatory submissions.</li><li>Collaborate with clinical researchers and other scientists.</li><li>Develop and maintain statistical programming code.</li><li>Stay up-to-date on the latest statistical methods and regulations.</li><li>Contribute to the development of new statistical methodologies.</li></ul></p><p><strong>Required Qualification and Skills:</strong><ul><li>Master's or PhD in biostatistics or a related field.</li><li>Experience in clinical trials and regulatory submissions.</li><li>Proficiency in statistical software (e.g., SAS, R).</li><li>Strong analytical and problem-solving skills.</li><li>Excellent communication and documentation skills.</li><li>Knowledge of drug development processes.</li></ul></p><p><strong>Benefits Included:</strong><ul><li>Competitive salary and benefits package.</li><li>Opportunities for professional development and career growth.</li><li>Work on meaningful projects that impact global health.</li><li>Collaborative and supportive work environment.</li><li>Health insurance and other employee benefits.</li></ul></p><p><strong>A Day in the Life:</strong>  A typical day involves data analysis, report writing, collaboration with other scientists, and staying current on new regulations and methodologies.</p>