<p><strong>What role you will play in team:</strong> You will be a key member of our biostatistics team, working on clinical trials and drug development projects.</p><p><strong>What you will do:</strong> You will design studies, analyze clinical trial data, and prepare reports for regulatory submissions.</p><p><strong>Key responsibility:</strong><ul><li>Design statistical analysis plans for clinical trials.</li><li>Analyze clinical trial data using appropriate statistical methods.</li><li>Prepare statistical reports for regulatory submissions.</li><li>Collaborate with other members of the clinical development team.</li><li>Stay up-to-date on new statistical methods and regulatory guidelines.</li><li>Present findings to internal and external stakeholders.</li></ul></p><p><strong>Required Qualification and Skills:</strong><ul><li>Master's or PhD in Biostatistics or Statistics.</li><li>1-3 years of experience in the pharmaceutical industry (preferred).</li><li>Strong programming skills in R or SAS.</li><li>Experience with clinical trial data analysis.</li><li>Knowledge of regulatory guidelines for clinical trials.</li></ul></p><p><strong>Benefits Included:</strong><ul><li>Competitive salary and benefits package.</li><li>Opportunities for career development within a global organization.</li><li>Challenging and rewarding work environment.</li><li>Opportunities to contribute to the development of new medicines.</li></ul></p><p><strong>A Day in the Life:</strong> A day would involve analyzing data, writing reports, attending meetings, collaborating with colleagues, and working on various projects related to clinical trials.</p>