Principal Biostatistician (Immunology) - FSP
IQVIA
Principal Biostatistician (Immunology) - FSP
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 stakeholdersCandidate 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 experienceIQVIA 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.comIQVIA 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.
Locations
- United Kingdom, Berkshire, Reading
- Serbia, Belgrade
- Austria, Vienna
- Hungary, Budapest
- Poland, Warsaw
- Netherlands, Amsterdam
- Ireland, Dublin
- Bulgaria, Sofia
- Germany, Hesse, Frankfurt
- Slovenia, Ljubljana – Dunajska
- Greece, Athens
- Spain, Madrid
- Belgium, Brussels-Capital Region, Brussels
- Czech Republic, Prague
- Slovakia, Bratislava
- Denmark, Copenhagen
- Sweden, Stockholm
Skills Required
- Phase IIintermediate
- SAP writingintermediate
Required 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 (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 (experience)
- 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. (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
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