Senior Director, Biostatistics Consulting

ICON

Uk, United Kingdom
Biostatistics consulting expertise
Clinical trial design and analysis
Regulatory agency negotiation
As a Senior Director, you will play a pivotal role in leading our biostatistics consulting practice by providing expert guidance on optimal statistical design, helping with regulatory agency negotiations, and guiding the strategic direction of clinical research programs in collaboration with therapeutic area experts

Job Summary

  • As a Senior Director, you will play a pivotal role in leading our biostatistics consulting practice by providing expert guidance on optimal statistical design, helping with regulatory agency negotiations, and guiding the strategic direction of clinical research programs in collaboration with therapeutic area experts.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and the company is committed to providing a workplace free of discrimination and harassment.

Matching Summary

As a Senior Director, you will play a pivotal role in leading our biostatistics consulting practice by providing expert guidance on optimal statistical design, helping with regulatory agency negotiations, and guiding the strategic direction of clinical research programs in collaboration with therapeutic area experts.

Skills & Requirements

Must-have

  • biostatistics consulting expertise
  • clinical trial design and analysis
  • regulatory agency negotiation
  • statistical strategy development
  • team leadership and management

Nice-to-have

  • Bayesian methodologies knowledge
  • cross-functional collaboration
  • client relationship building
  • innovative problem-solving
  • excellent communication skills

Key Requirements

  • Advanced degree in biostatistics or related field
  • Significant experience in biostatistics consulting
  • Extensive clinical trial design and analysis experience
  • Proven leadership of biostatistics teams
  • Experience authoring regulatory submission statistical sections

Work Rights

Not specified

Tailored Resume

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