Senior Biostatistician – Oncology (FSP -Permanent Homebased)

IQVIA; Paris; À distance; EUR 80 000 - 100 000; Plein temps

Résumé du poste

A global clinical research organization is seeking an experienced Senior Biostatistician to support late-phase oncology trials. This permanent, home-based position involves overseeing trial designs, statistical analysis plans, and regulatory submissions. Candidates should possess a Master's or PhD, with at least 5 years of relevant clinical trial experience. Join a collaborative environment dedicated to improving cancer treatment outcomes.

Prestations

Flexibility of remote work

Collaboration with a leading team

Exposure to cutting-edge oncology research

Qualifications

• 5+ years of experience in clinical trials, particularly in oncology.
• Proven experience working on registrational studies and regulatory submissions.
• Strong knowledge of CDISC standards, particularly ADaM and SDTM.

Responsabilités

• Lead statistician on global late-phase registration trials in oncology.
• Independently contribute to study design and statistical analysis plans.
• Ensure timely and accurate delivery of statistical deliverables.

Connaissances

SAS programming

Statistical analysis

CDISC standards

Communication skills

Formation

Master’s or PhD in Biostatistics, Statistics, or related field

Description du poste

We are seeking an experienced and proactive Senior Biostatistician to join our FSP team, supporting a global pharmaceutical client. This is a permanent, home-based position offering the opportunity to work on late-phase global oncology trials, with a focus on hematology and regulatory submissions.

Key Responsibilities

• Serve as the lead statistician on global late-phase registration trials, particularly in oncology (hematology preferred).
• Independently contribute to study design, statistical analysis plans (SAPs), and regulatory submission strategies.
• Participate in study team meetings, providing statistical guidance and collaborating with cross-functional teams.
• Address health authority questions and support responses with appropriate statistical analyses and documentation.
• Perform hands-on statistical programming to derive outputs and summary statistics using ADaM and SDTM datasets.
• Ensure timely and accurate delivery of statistical deliverables in compliance with regulatory standards.

Required Qualifications

• Advanced degree (Master’s or PhD) in Biostatistics, Statistics, or a related field.
• 5+ years of experience in clinical trials, with a strong focus on oncology (hematology and late-phase preferred).
• Proven experience working on registrational studies and regulatory submissions.
• Strong knowledge of CDISC standards, particularly ADaM and SDTM.
• Proficiency in SAS programming and ability to perform hands-on statistical analyses.
• Excellent communication skills and ability to work independently in a global, cross-functional environment.

Preferred Experience

• Prior involvement in FDA / EMA submissions.
• Experience addressing regulatory agency queries.
• Familiarity with real-world evidence and observational studies is a plus.

Why Join Us?

• Work on high-impact global studies with a focus on improving cancer treatment outcomes.
• Be part of a collaborative and innovative team environment.
• Enjoy the flexibility of remote work with a permanent contract.
• Gain exposure to regulatory strategy and cutting-edge oncology research.

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