Associate Director, Statistical Science - Biostatistics

Responsibilities

• Lead the delivery and oversight on multiple studies/indications within a project, potentially as a Global Project Statistician for a standard drug project.
• Lead the statistical thinking and contributions to the delivery of studies, development plans, regulatory strategy, health technology assessment and/or commercial activities.
• Direct project work, including statistical staff and/or CRO partners, to ensure delivery to standards, quality and time.
• Develop design options and provide high-quality decision support to allow the business to make informed decisions about a study or project.
• Measure the benefit, risk, value and uncertainty of the latest asset/product profile.
• Investigate and apply novel statistical approaches, for relevant statistical issues and/or regulatory guidance and/or value demonstration, including modelling and simulation.
• Coach and support the training of statistics staff.

Requirements

• MSc/PhD in Statistics, Mathematics (containing a substantial statistical component), or recognized equivalent to stats MSc
• 5+ years of experience of pharmaceutical development, data analysis and interpretation and experience of program design.
• Knowledge of programming in R and/or SAS.
• Knowledge of the technical and regulatory requirements related to the role.
• Excellent collaboration skills to work across functional boundaries.
• Apply statistical expertise to complex problems focusing on quality.

Qualifications

• Desirable: Project Management Skills
• Desirable: Proficiency in SAS and R/Python languages

Pay

The annual base pay for this position ranges from $151,000 to $227,000.

Schedule

N/A

Benefits

Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.