Lead one or several late phase studies or lead an indication for a complex compound.
Provide high-quality input into study design, setup, and conduct and be accountable for statistical aspects of the study.
Prepare statistical methods, contribute to result interpretation, and ensure statistical integrity in clinical study reports and publications; perform exploratory and ad-hoc analyses to support study or project objectives.
Plan, monitor and manage study activities, timelines to align practices in compliance with Sanofi SOPs and EGDS standards.
Mentor junior project team members and promote a culture of productive teamwork, quality, operational efficiency, and innovation.
Oversee execution of statistical analyses, coordinating with programmers as needed.
Develop productive collaboration with other functions in the aligned project team.
Requirements
PhD in statistics or related discipline, with minimum 1 year of pharmaceutical experience in clinical development
MS in statistics or related discipline, with minimum 3 years of pharmaceutical experience in clinical development
Broad knowledge and good understanding of advanced statistical concepts and techniques; being able to do advanced statistical analyses using SAS or R
Demonstrated strong project management, interpersonal and communication skills.
Experience of participation to cross company &/or academia workings or special interest groups