The Role

We are seeking an experienced Statistician to join the team in a permanent position based in the US or Canada. This is a client-facing role that combines advanced statistical expertise with project leadership responsibilities. You will play a key role in designing and analyzing clinical trials, managing timelines, and ensuring regulatory compliance.

Key Responsibilities

• Provide statistical input into clinical trial design, analysis plans, and regulatory submissions

• Act as the primary statistical contact for clients, ensuring clear communication and strong relationships

• Lead projects from a statistical perspective, managing deliverables and timelines

• Oversee and review statistical analyses, ensuring accuracy and compliance with regulatory standards

• Collaborate with cross-functional teams including programming, data management, and clinical operations

• Contribute to process improvement and best practices within the biometrics team

Qualifications

• Minimum 3 years of industry experience (CRO, consulting, or pharma)

• Strong knowledge of clinical trial methodology and regulatory requirements

• Proven experience in a client-facing role with project management responsibilities

• Proficiency in statistical software (SAS is a plus, but not mandatory)

• Excellent communication, leadership, and problem-solving skills

• Advanced degree in Statistics, Biostatistics, or a related field

The Offer

• Competitive salary and comprehensive benefits package (401k)

• Opportunity to work on global projects across diverse therapeutic areas

• Professional growth through career development programs and continuous learning

• Collaborative and innovative work environment

Send us your CV below and let us know why you would be a great fit for the opportunity.