In this role you provide strategic statistical leadership for oncology clinical development programs, with emphasis on hematologic malignancies. You collaborate with cross-functional teams to deliver high-quality statistical outputs that meet regulatory standards. You guide study design, methodology, and interpretation of results, communicating complex analyses to diverse stakeholders. You drive timely, compliant deliverables and quality across the development lifecycle. This opportunity combines leadership, impact on patient outcomes, and the chance to influence oncology programs at a global services leader.
autonomy and balance
flexible hours
Provide principal-level biostatistics leadership for oncology development programs and studies
Serve as the primary statistical representative on assigned trials and contribute to statistical activities across studies
Review and QC SDTM datasets and deliverables to ensure CDISC compliance
Collaborate with Statistical Programming, Data Management, Clinical Operations, and Regulatory teams to ensure timely, accurate outputs

Assist in interpretation and communication of study results to cross-functional stakeholders
Ensure statistical deliverables meet quality, regulatory, and timeline expectations
Summarize and communicate statistical concepts and recommendations to technical and non-technical audiences
Contribute to study design discussions, protocol development, and methodological considerations as needed
Advanced experience as a Principal Biostatistician in pharma, biotech, or CRO
Strong oncology experience, with hematological malignancies experience (e.g., multiple myeloma, leukemia, lymphoma)
Expertise in CDISC standards, especially SDTM, including QC oversight of SDTM datasets
Proven ability to work in cross-functional teams and influence stakeholders
Excellent verbal and written communication skills
Solid understanding of statistical principles and clinical trial methodology
J-18808-Ljbffr

Principal Biostatistician

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(PI) Addetti/e alle pulizie