Senior Biostatistician – Oncology (FSP -Permanent Homebased)

IQVIA; City Of London; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading global healthcare service provider is seeking an experienced Senior Biostatistician to join their FSP team. This role involves leading statistical efforts on late-phase oncology trials, particularly hematology, and contributing to regulatory submissions. The ideal candidate will have over 5 years of clinical trial experience, strong knowledge of CDISC standards, and SAS programming skills. Enjoy flexibility with a permanent home-based position.

Benefits

Flexible remote work

Collaborative team environment

Exposure to cutting-edge oncology research

Qualifications

• 5+ years of experience in clinical trials, particularly in oncology.
• Proven experience working on registrational studies and regulatory submissions.
• Strong knowledge of CDISC standards.

Responsibilities

• Lead statistician on global late-phase registration trials.
• Contribute to study design and statistical analysis plans.
• Participate in study team meetings providing statistical guidance.

Skills

Hands-on statistical programming

SAS programming

Excellent communication skills

Knowledge of CDISC standards

Education

Advanced degree in Biostatistics or related field

Tools

ADaM

SDTM

Job description

Overview

We are seeking an experienced and proactive Senior Biostatistician to join our FSP team, supporting a global pharmaceutical client. This is a permanent, home-based position offering the opportunity to work on late-phase global oncology trials, with a focus on hematology and regulatory submissions.

Key Responsibilities

• Serve as the lead statistician on global late-phase registration trials, particularly in oncology (hematology preferred).
• Independently contribute to study design, statistical analysis plans (SAPs), and regulatory submission strategies.
• Participate in study team meetings, providing statistical guidance and collaborating with cross-functional teams.
• Address health authority questions and support responses with appropriate statistical analyses and documentation.
• Perform hands-on statistical programming to derive outputs and summary statistics using ADaM and SDTM datasets.
• Ensure timely and accurate delivery of statistical deliverables in compliance with regulatory standards.

Required Qualifications

• Advanced degree (Master’s or PhD) in Biostatistics, Statistics, or a related field.
• 5+ years of experience in clinical trials, with a strong focus on oncology (hematology and late-phase preferred).
• Proven experience working on registrational studies and regulatory submissions.
• Strong knowledge of CDISC standards, particularly ADaM and SDTM.
• Proficiency in SAS programming and ability to perform hands-on statistical analyses.
• Excellent communication skills and ability to work independently in a global, cross-functional environment.

Preferred Experience

• Prior involvement in FDA/EMA submissions.
• Experience addressing regulatory agency queries.
• Familiarity with real-world evidence and observational studies is a plus.

Why Join Us?

• Work on high-impact global studies with a focus on improving cancer treatment outcomes.
• Be part of a collaborative and innovative team environment.
• Enjoy the flexibility of remote work with a permanent contract.
• Gain exposure to regulatory strategy and cutting-edge oncology research.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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