Principal Biostatistician

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

What you will be doing :

• Serve as the responsible biostatistician on clinical trials.
• Contribute to clinical study protocols.
• Develop Statistical Analysis Plans and / or perform senior quality review of statistical analysis plans.
• Review and interpret results from simple to complex clinical studies.
• Provide input in the development and review of CRFs.
• Perform lead review and QC of TFLs.
• Critically review derived datasets specifications and datasets (ADaM).
• Present key results.
• Contribute to clinical study reports.
• Review randomization specifications and schemes.
• Oversee outsourced trials from a Biostatistics perspective.
• Contribute to press releases and scientific publications.

You are :

• PhD in statistics, biostatistics, or related field with 5+ years of experience in CRO or pharmaceutical companies OR a Master’s degree with 10+ years of experience.
• Thorough knowledge of CDISC standards and regulatory requirements.
• Experience with Phase 2 and 3 studies.
• Proficiency in R programming, ESTIMANDS, adaptive designs, and writing SAPs.
• Experience in analysis creation for publications.
• Strong leadership and communication skills.
• Knowledge of ADaM and TFL programming.

Why ICON?

We offer a comprehensive reward package, including competitive pay, variable incentives, and employee benefits. We are committed to continuous learning and professional development. ICON is an equal opportunity employer dedicated to a discrimination-free workplace. If you require accommodations during the application process, please let us know. We encourage all qualified individuals to apply, regardless of whether you meet every requirement.

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