Principal Biostatistician (Immunology) - FSP

IQVIA

Reading

On-site

GBP 90,000 - 130,000

Full time

14 days+
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Job summary

IQVIA seeks a Principal Biostatistician to provide end-to-end statistical leadership across Phase II and Phase III studies. You will work closely with cross-functional stakeholders in a fast-paced, global environment to drive SAP development, trial analysis, and integrated program statistics.

The role emphasizes independent execution, proactive collaboration with Clinical, Programming, and Regulatory teams, and delivery of high‑quality outputs within timelines.

Qualifications

  • Strong experience as a Principal Biostatistician (Pharma or CRO).
  • End-to-end knowledge of Phase II and III studies.
  • Proven expertise in SAP writing and reviewing.
  • Ability to work independently with minimal supervision.
  • Proactive, solution-oriented communicator.
  • Immunology TA experience – good to have, not mandatory.
  • Strong R Programming experience.

Responsibilities

  • Provide Principal-level Biostatistics support for Phase II–III clinical trials
  • Independently lead SAP authoring and review
  • Support integration activities across studies and programs
  • Act as a proactive statistical partner to Clinical, Programming, and Regulatory teams
  • Ensure delivery of high‑quality, compliant statistical outputs within timelines
  • Communicate clearly and confidently with internal and external stakeholders

Skills

Biostatistics
R programming
SAP writing
Phase II–III experience
Stakeholder communication
Independent work

Tools

R

Job description

As a Principal Biostatistician, you will provide end‑to‑end statistical leadership and integration support across Phase II and Phase III studies, working closely with cross‑functional stakeholders in a fast‑paced, global environment.

Key Responsibilities
  • Provide Principal‑level Biostatistics support for Phase II–III clinical trials
  • Independently lead SAP authoring and review
  • Support integration activities across studies and programs
  • Act as a proactive statistical partner to Clinical, Programming, and Regulatory teams
  • Ensure delivery of high‑quality, compliant statistical outputs within timelines
  • Communicate clearly and confidently with internal and external stakeholders
Candidate Requirements
  • Strong experience as a Principal Biostatistician (Pharma or CRO)
  • End‑to‑end knowledge of Phase II and III studies
  • Proven expertise in SAP writing and reviewing
  • Ability to work independently with minimal supervision
  • Proactive, solution‑oriented communicator
  • Immunology TA experience – good to have, not mandatory
  • Strong R Programming experience

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. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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