Lead Biostatistician, Oncology Trials & Hematology

IQVIA; Netherlands; On-site; EUR 120,000 - 180,000; Full time

Job summary

IQVIA is seeking a Principal Biostatistician to provide strategic statistical leadership for oncology clinical trials, with a focus on hematological malignancies including multiple myeloma, leukemia, and lymphoma. You will collaborate with cross-functional teams to deliver high-quality statistical support across the development lifecycle, ensuring regulatory compliance.

The role requires extensive experience as a principal statistician in pharma/biotech/CRO settings, strong CDISC/SDTM knowledge,

Qualifications

• Advanced experience as a Principal Biostatistician in Pharma/Biotech/CRO environments.
• Strong oncology clinical development experience.
• Expertise in hematological malignancies (myeloma, leukemia, lymphoma).
• CDISC standards knowledge, including SDTM.
• Experience QC'ing SDTM datasets and outputs.
• Ability to influence cross-functional teams.
• Excellent verbal and written communication skills.

Responsibilities

• Provide Principal-level Biostatistics leadership for Oncology clinical development programs and studies.
• Lead statistical activities across trials, acting as the primary statistical representative on assigned studies.
• Review and quality-control SDTM datasets and deliverables to CDISC standards.
• Collaborate with Statistical Programming, Data Management, Clinical Operations, and Regulatory teams to ensure timely delivery of outputs.
• Support interpretation and communication of study results to cross-functional stakeholders.
• Ensure all statistical deliverables meet quality, regulatory, and timeline expectations.
• Communicate statistical concepts and recommendations to technical and non-technical audiences.
• Contribute to study design discussions, protocol development, and statistical methodology as required.

Job description

IQVIA is seeking a Principal Biostatistician to provide strategic statistical leadership for oncology clinical trials, with a focus on hematological malignancies including multiple myeloma, leukemia, and lymphoma. You will collaborate with cross-functional teams to deliver high-quality statistical support across the development lifecycle, ensuring regulatory compliance.

The role requires extensive experience as a principal statistician in pharma/biotech/CRO settings, strong CDISC/SDTM knowledge,