Senior Biostatistician – Oncology (FSP -Permanent Homebased)

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

Job summary

A leading clinical research organization is seeking a Senior Biostatistician to support late-phase global oncology trials. This permanent, home-based position involves leading statistical analyses and regulatory submissions, requiring an advanced degree and over 5 years of relevant experience. The role promises an opportunity to work on impactful studies while ensuring compliance with regulatory standards.

Benefits

Flexible remote work

Collaboration with an innovative team

Opportunity to work on global studies

Qualifications

• 5+ years of experience in clinical trials, especially in oncology.
• Proven experience on registrational studies and regulatory submissions.
• Familiarity with FDA/EMA submissions is a plus.

Responsibilities

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

Skills

Statistical analysis

SAS programming

Strong communication skills

Knowledge of CDISC standards

Ability to work independently

Education

Advanced degree (Master’s or PhD) in Biostatistics or Statistics

Tools

SAS

Job description

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 intelligent connections to accelerate the development and commercialization of innovative medical treatments to help 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.

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