Quanticate
Pharmaceuticals
SeniorStatisticianI/II
Neural analysis suggests this role is
optimal for Senior candidates.
“Senior Statistician I/II at Quanticate. Skills: Statistics, Programming, Clinical trials. Design clinical studies. Analyse clinical studies”
Industry & Context.
Problem solving
What They're Looking For.
Must Have
MSc in Statistics, Statistician experience in CRO, Experience across clinical trial phases, Experience across therapeutic areas, Analytical and problem solving capability, Clear written and verbal communication skills
Nice to Have
PhD preferred, Specific ML framework experience, Cloud platform certs
What You'll Do.
Design clinical studies
Analyse clinical studies
Input into Statistical Analysis Plans
Calculate sample size
Program derived datasets
Quality control derived datasets
Program CDISC compliant datasets
Quality control CDISC compliant datasets
Peer review statistical deliverables
Peer review programming deliverables
Ensure outputs meet internal SOPs
Ensure outputs meet client requirements
Ensure outputs meet regulatory expectations
Manage assigned project work
Communicate with sponsors
Line manage team members
Provide performance feedback
Supervise team members
Oversight resource allocation
Contribute to performance reviews
Monitor functional KPIs
Deputise for Senior Statistical Programmer
Interact with clients
Contribute to study calls
Contribute to project meetings
How You'll Work.
Team & Collaboration
Lead Statisticians; Lead Programmers; Clients
Communication Scope
Explain statistical concepts
Process & Methodology
Project management
Full Job Description
If you are an experienced Senior Statistician who is comfortable moving between statistical leadership and hands on programming, this role offers the scope and responsibility to match your expertise. We are looking for a Senior Statistician to act as a senior technical resource across both statistics and programming functions, with primary alignment to the statistics group. You will play a central role in delivering high quality clinical trial outputs while supporting, reviewing and strengthening the work of others. ### What you will be responsible for You will contribute at a senior level across the full clinical trial reporting lifecycle. This includes: * Designing and analysing clinical studies, including input into protocols, Statistical Analysis Plans and sample size calculations * Programming and quality controlling derived datasets and CDISC compliant datasets * Producing and reviewing Tables, Listings and Figures * Providing peer review of statistical and programming deliverables * Ensuring all outputs meet internal SOPs, client requirements and regulatory expectations You will manage assigned project work independently, communicate clearly with sponsors when required, and flag risks that could affect timelines or data quality. High standards and attention to detail are essential. ### Technical expertise required You will bring: * Strong grounding in statistical principles and modelling * Advanced proficiency in SAS and R for dataset and TLF production * Excellent knowledge of CDISC standards * A solid understanding of ICH/GCP guidelines and the regulatory environment * Experience across multiple study phases and therapeutic areas This role requires someone who understands not just how to produce outputs, but why they are structured the way they are, and how they will be scrutinised in a regulatory setting. ### Leadership and collaboration You will line manage assigned team members, providing mentorship, training and performance feedback. Responsibilities in
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