Senior Biostatistician

at  ICON

As a Senior Biostatistician you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

WHY ICON?

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles

• Ability to perform Study Statistician role with minimal supervision
• Demonstrates strong statistical expertise with a good understanding of more complex design of experiments and inference methodologies (where applicable awareness / knowledge of Bayesian, Futility &
• Predictive Inference, Estimands, Missing Data etc.)
• Where required, ability to actively participate in matrix team meetings
• Applies standard processes to tasks, ensuring that deliverables are accurate, high quality and met according to agreed timelines
• Extensive working knowledge of GxP, ICH, internal GSK processes and external regulations (as applicable)
• Quality Control (QC) of other people’s work under supervision
• Under supervision:
• Supports design, analysis and interpretation, uses a wide range of statistical approaches and/or applicable software to explore options
• Authors analysis plans and prepares statistical inputs to key documents and presentation materials
• Contributes to the development of statistical strategy at a study-level, which may be shared with stakeholders