Senior biostatistician

Profile Summary

Functional lead of multiple moderate to high complex studies ; provide input to statistical components of clinical studies (e.g. protocol, mock shells, SAP text, programmed deliverables). Contribute to the development of more junior biostatisticians.

8 Years of Experience and Exhibit the Following Traits:

• Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated Functional Knowledge:
• Advanced functional knowledge level of Biostatistics. Business Expertise:
• Ability to apply advanced knowledge of best practices, and understanding of customer needs, and use this knowledge to add value. May include creation and delivery of training materials of moderate complexity. Leadership:
• Functional lead of multiple moderate to high complex studies, and act as a mentor for colleagues. Problem Solving:
• Solve complex problems; take a new perspective on existing solutions; exercise judgement based on the analysis of multiple sources of information. Impact:
• Establish approach and lead resources to achieve operational and strategic plans. Impact is focused on medium-term goals. Work is done independently, but subject to assessment.
• Adapt style and use persuasion in delivering messages. Issues may be complex, audience perspectives may be divergent, and information may be non-routine in nature.

What You Will Do:

• As a Senior Biostatistician II at ICON, you will lead the design, analysis, and interpretation of statistical data for clinical trials.

Your experience in biostatistics will be key in delivering high-quality outcomes and mentoring colleagues.

Key responsibilities include:

• Designing and implementing statistical analyses for clinical trials, including the development of statistical analysis plans and interpretation of results.
• Collaborating with cross-functional teams to define study objectives, data requirements, and statistical methodologies.
• Providing expert statistical guidance and support for the development of clinical trial protocols and data analysis strategies.
• Ensuring compliance with regulatory standards and industry best practices in statistical analysis and reporting.
• Mentoring and supporting junior statisticians, fostering a collaborative and innovative environment