Senior Biostatistician

Role:

• Contribute with your statistical expertise to the design and analysis of one or more clinical trials or the clinical development plan of one compound/program.
• Will closely collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials and contribute to HA submissions
• Will report to a franchise team leader, within the Biostatistics and Statistical Modelling organisation
• Will carry out functional responsibilities in accordance with applicable company guidelines and regulatory requirements

Education and Experience:

• You have a master or doctorate (Ph.D.) degree in Statistics or related field with a minimum of 5+ years of experience (which may include doctoral research in field of biostatistics) (Master is a required qualification)
• You have expertise in drug development, with a demonstrated track record of advanced knowledge of biostatistics and strong command of its application to clinical trials
• Demonstrates ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical trials
• You are proficient in statistical software (SAS and/or R);
• You are able to collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials
• You can clearly explain complex statistical concepts in written and spoken English
• You are a team-player with focused attitude
• You are able to work autonomously as part of a cross-disciplinary team in a dynamic surrounding of a fast-growing biotech company with challenging timelines

Knowledge, Skills and Abilities:

• eCRT and Define knowledge
• Proactive in nature
• Project Lead abilities experience of working with cross functional teams and managing
• TA experience is preferable ( Immunology)
• Exposure to regulatory related work
• Exposure to latest Stat models and design approaches will be preferred
• Proactive communication