13 hours ago
• Provide comprehensive statistical support throughout clinical studies • Conduct statistical analyses and interpret results • Engage with regulatory bodies such as the FDA and EMEA • Extensive hands-on experience in statistical analysis using SAS • Actively engage with clients to understand their statistical and analytical needs • Responsible for creating and updating Standard Operating Procedures (SOPs)
• MSc or PhD in Biostatistics or Statistics • 10+ years of experience as Biostatistician in a CRO/Pharma/Biotech company • 3+ years of experience leading a team of biostatisticians and statistical programmers • Strong written and verbal communication skills in English • Proficient in SAS, R, or Python • Knowledge of regulatory guidelines and statistical methodology related to clinical development • Strong knowledge of ICH guidelines
• Competitive salary • Paid time off • Healthcare benefits • Retirement benefits
Apply Now