Principal Biostatistician (Oncology) - Fsp

Descrizione dell’offerta di lavoro

Questa posizione è in IQVIA

Il processo di selezione sarà interamente gestito IQVIA.

Questa opportunità è disponibile in Reading - United Kingdom, Belgrade - Serbia, Rome - Italy, Paris - France, Vienna - Austria, Budapest - Hungary, Amsterdam - Netherlands, Dublin - Ireland, Sofia - Bulgaria, Frankfurt - Germany, Athens - Greece, Ljubljana - Slovenia, Madrid - Spain, Brussels - Belgium, Bratislava - Slovakia, Prague - Czech Republic, Copenhagen - Denmark, Stockholm - Sweden.

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As a

Principal Biostatistician , you will provide strategic statistical leadership for

Oncology clinical trials , with a particular focus on

hematological malignancies

including

multiple myeloma, leukemia, and lymphoma . You will work closely with cross-functional teams to deliver high-quality statistical support across the clinical development lifecycle, ensuring compliance with regulatory and industry standards.

Key Responsibilities

Provide Principal-level Biostatistics leadership for Oncology clinical development programs and studies

Lead and contribute to statistical activities across clinical trials, acting as the primary statistical representative on assigned studies

Review and provide quality control oversight of

SDTM datasets and associated deliverables , ensuring compliance with

CDISC standards

Collaborate closely with Statistical Programming, Data Management, Clinical Operations, and Regulatory teams to ensure accurate and timely delivery of statistical outputs

Support the interpretation and communication of study results to cross-functional stakeholders

Ensure all statistical deliverables meet quality, regulatory, and timeline expectations

Effectively communicate statistical concepts, analyses, and recommendations to both technical and non-technical audiences

Contribute to study design discussions, protocol development, and statistical methodology as required

Candidate Requirements

Advanced experience as a

Principal Biostatistician

within a Pharmaceutical, Biotechnology, or CRO environment

Strong experience within

Oncology clinical development

Demonstrated expertise in

hematological malignancies , including

multiple myeloma, leukemia, and/or lymphoma

Strong knowledge and practical application of

CDISC standards , including

SDTM

Experience performing or overseeing

QC of SDTM datasets and related outputs

Proven ability to work effectively within cross-functional teams and influence key stakeholders

Excellent verbal and written communication skills

Strong understanding of statistical principles and clinical trial methodology

Preferred Qualifications

Experience serving as

Lead Study Statistician

within a cross-functional clinical development team

Knowledge and experience in

clinical trial statistical design

and study planning

Experience supporting regulatory submissions and interactions with health authorities

Familiarity with advanced statistical programming tools and industry-standard processes

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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