Consultant – Clinical Biostatistician, RWE

Jobtailor; Paris; Sur place; EUR 55 000 - 85 000; Plein temps

Résumé du poste

Jobtailor is seeking a Senior Clinical Statistician to lead statistical sections of SAPs, draft analyses, and ensure CDISC-compliant deliverables in collaboration with physicians and clinical teams.

You will design methodologies, calculate sample sizes, perform SAS/R analyses, and ensure on-time delivery while maintaining high quality standards.

Qualifications

• Master’s degree in Statistics (BAC+5) required.
• Minimum 3 years of experience in clinical statistics or RWD statistics.
• Strong background in biostatistics.
• Proficiency in SAS and R programming.
• Solid knowledge of clinical development and statistical methodologies.
• Fluent English required.
• Excellent communication and coordination with diverse stakeholders.

Responsabilités

• Define the most appropriate statistical methodology.
• Participate in selecting analysis strategies and calculate the required sample size.
• Draft, review and validate the statistical sections of clinical protocols and the SAP.
• Contribute to writing synopses and scientific documents.
• Perform analyses and carry out statistical programming in SAS or R.
• Ensure the production and delivery of deliverables and datasets on time, in accordance with quality standards and in CDISC format.
• Be responsible for the completion, filing and compliance of the eTMF for the statistical section.
• Summarize, model and interpret the results of clinical analyses.
• Collaborate closely with physicians and clinical teams on a day-to-day basis.
• Review and approve all external scientific communications related to the studies.

Connaissances

Biostatistics

Clinical data / RWD

SAS

R

Statistical methods

CDISC

eTMF

Communication

English

Formation

Master's degree in Statistics

Outils

SAS

R

Description du poste

Responsibilities

• Define the most appropriate statistical methodology
• Participate in selecting analysis strategies and calculate the required sample size
• Draft, review and validate the statistical sections of clinical protocols and the Statistical Analysis Plan (SAP)
• Contribute to writing synopses and scientific documents
• Perform analyses and carry out statistical programming in SAS or R
• Ensure the production and delivery of deliverables and datasets on time, in accordance with quality standards and in CDISC format
• Be responsible for the completion, filing and compliance of the eTMF for the statistical section
• Summarize, model and interpret the results of clinical analyses
• Collaborate closely on a day-to-day basis with physicians and clinical teams
• Review and approve all external scientific communications related to the studies

Requirements

• Strong background in biostatistics
• Proven expertise with clinical data or real‑world data (RWD)
• Master’s degree (Bac+5 or equivalent) in Statistics
• Minimum 3 years of experience in clinical statistics and/or RWD statistics
• Proficiency in SAS & R programming
• Solid knowledge of overall clinical development and statistical methodologies
• Rigour and strong organizational skills
• Excellent communication and coordination skills with diverse stakeholders
• Fluent English required