Senior biostatisticien

JR France; Levallois-Perret; Sur place; EUR 70 000 - 90 000; Plein temps

Résumé du poste

A leading CRO is seeking a Senior Biostatistician in Levallois-Perret. The role involves conducting statistical activities and ensuring project progression in a dynamic environment. Candidates should have advanced degrees in statistics, extensive experience in the pharmaceutical sector, and proficiency in SAS and R.

Qualifications

• Higher education in statistics (ENSAI, ISUP, Master’s or PhD).
• At least 6 years of experience in the pharmaceutical industry/CRO.
• Fluent in English and bilingual in French.

Responsabilités

• Conduct statistical activities in study design and oversight.
• Supervise outsourced statistical activities to CROs.
• Draft and review statistical documentation.

Connaissances

Statistical analysis

Project management

Communication

Formation

Master’s or PhD in statistics

Outils

SAS

R

Description du poste

Senior biostatistician, Levallois-Perret

Are you passionate about Life Sciences and Clinical Research? Do you want to evolve in a dynamic and collaborative international environment where your expertise directly impacts the lives of millions? We are seeking a senior biostatistician to bring their expertise to statistical activities and ensure the smooth progression of projects.

Your responsibilities will include:

1. Conducting statistical activities in study design: sample size calculation, design choices, evaluation criteria, estimand definition, etc.
2. Being the point of contact for all statistical matters and participating in project/study meetings.
3. Participating in the selection of subcontractors by establishing specifications and evaluating proposals.
4. Drafting and reviewing the synopsis, protocol, statistical analysis plan, randomization specifications, and other study documentation.
5. Supervising outsourced statistical activities to CROs and ensuring compliance with cost, timeline, and quality requirements.
6. Verifying the presence of all statistical documentation in the Trial Master File (TMF).

Qualifications include:

• Higher education in statistics (ENSAI, ISUP, Master’s or PhD in statistics).
• At least 6 years of experience in the pharmaceutical industry/CRO in a similar role, involved from early clinical development stages (oncology).
• Proficiency in SAS and R software.
• Solid knowledge of international scientific and regulatory guidelines (ICH, EMA, FDA, ...).
• Fluent in English (reading, writing, speaking) and bilingual in French.

We are one of the world leaders in CROs, committed to excellence, with expertise and flexibility to conduct clinical studies. We work with pharmaceutical, biotechnological, cosmetic companies, and more, providing innovative and adaptable solutions. Operating across 10 countries on 3 continents with over 1000 talented professionals, we are dedicated to advancing clinical research and fostering gender parity in our strategic development.