Senior Biostatistician – Oncology (FSP -Permanent Homebased)

IQVIA; Paris; À distance; EUR 70 000 - 90 000; Plein temps

Résumé du poste

A leading global provider of clinical research services is seeking a Senior Biostatistician for a permanent, home-based position. The role involves leading late-phase global oncology trials, focusing on statistical analyses and regulatory submissions. The position offers flexibility and a chance to work on impactful studies that improve cancer treatment outcomes.

Prestations

Flexible remote work

Collaborative and innovative team environment

Exposure to regulatory strategy

Qualifications

• 5+ years of experience in clinical trials with oncology focus.
• Proficiency in SAS programming and statistical analyses.
• Experience with registrational studies and regulatory submissions is a must.

Responsabilités

• Lead statistician on global late-phase registration trials.
• Contribute to study design and regulatory submission strategies.
• Perform statistical programming and ensure compliance with regulatory standards.

Connaissances

Statistical analysis

SAS programming

Communication skills

Formation

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

Outils

CDISC standards

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