Job Description

Responsibilities:

• 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 organization.
• Will carry out functional responsibilities in accordance with applicable company guidelines and regulatory requirements.

Requirements:

• You have a master or doctorate (Ph.D.) degree in Statistics or related field with a minimum of 5 years' experience (which may include doctoral research in the 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 can 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 can work autonomously as part of a cross-disciplinary team in a dynamic surrounding of a fast-growing biotech company with challenging timelines.

Skills:

• 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.

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