Principal Statistician

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Requirements:

• MSc in Biostatistics, Statistics or equivalent.
• Strong statistical expertise with experience in clinical trials.
• Experience in SAS programming.
• Extensive knowledge of regulatory requirements for clinical trials.
• Strong project management and leadership skills with experience leading large-scale projects.
• Excellent verbal and written communication skills.
• Ability to work independently and as part of a team.
• Willingness to travel when needed.

Responsibilities:

• Serve as lead statistician for clinical trials including planning, analysing, and reporting, ensuring that all deliverables are met on time and to a high level of quality.
• Develop and validate statistical models and analyses based on study protocols.
• Write statistical analysis plans and reports.
• Provide guidance and mentorship to other statisticians in the group.
• Collaborate with cross-functional teams to develop study protocols and ensure they meet regulatory requirements.
• To potentially take line management responsibility for junior statisticians within the team.
• To lead statistical consultancy projects as required, providing expert statistical advice on all statistical aspects of study design and conduct.
• Perform ad hoc statistical duties as required.