Job Details
Senior Statistician
6192
Posted: 23/04/2026
- £Competitive
- Home Based - US, United States
- Permanent
Senior Biostatistician | Global CRO | Permanent | Remote – US |
We’re partnering with a fast-growing, highly innovative CRO that’s redefining how clinical trials are delivered. Their mission is simple but ambitious, make clinical trials faster, more efficient, and more accessible using AI-driven approaches. If you’re looking for a role where you can genuinely have impact this may be of interest.
The Opportunity
As a Senior Statistician you will take ownership of clinical studies end-to-end, with a particular focus on Phase II & III trials.
This is a hands-on, high-impact role where you’ll:
What You’ll Be Doing
What They’re Looking For
Why Join?
Interested?
If you’re interested please apply or reach out directly for a confidential conversation.
We’re partnering with a fast-growing, highly innovative CRO that’s redefining how clinical trials are delivered. Their mission is simple but ambitious, make clinical trials faster, more efficient, and more accessible using AI-driven approaches. If you’re looking for a role where you can genuinely have impact this may be of interest.
The Opportunity
As a Senior Statistician you will take ownership of clinical studies end-to-end, with a particular focus on Phase II & III trials.
This is a hands-on, high-impact role where you’ll:
- Lead studies from design through to submission
- Work across a variety of therapeutic areas
- Act as a key statistical expert internally and externally
- Contribute to a growing, collaborative biostatistics function
What You’ll Be Doing
- Leading statistical strategy, design, and analysis for clinical trials
- Taking ownership of studies end-to-end
- Delivering high-quality statistical programming in R
- Supporting and contributing to regulatory submissions
- Reviewing ADaMs and SDTMs for submission packages
- Acting as a subject matter expert across cross-functional teams
- Mentoring junior statisticians and helping shape best practices
What They’re Looking For
- Minimum of 5+ years’ experience in biostatistics within clinical research
- Strong R programming skills
- Solid understanding of CDISC standards and regulatory submissions (FDA experience preferred)
- Experience leading studies, ideally Phase II–III
- Ability to manage multiple projects and work independently
- Most importantly they’re looking for someone with a great personality, strong track record, and the confidence to lead and collaborate effectively.
Why Join?
- Be part of a high-growth, AI-driven CRO disrupting the industry
- Work in a high-impact, mission-driven environment
- Gain real ownership and visibility across studies
- Collaborate with a smart, no-ego team
- Play a direct role in helping bring new treatments to patients faster
Interested?
If you’re interested please apply or reach out directly for a confidential conversation.
Aimee Weston
Principal Consultant in Biostatistics
Apply for this role
Recruitment