Senior Biostatistics Manager (Remote from France)

Medium; Tremblay-en-France; Hybride; EUR 70 000 - 90 000; Plein temps

Résumé du poste

A leading healthcare consulting firm is seeking a Senior Biostatistics Manager for their Tremblay-en-France office. This role involves leading complex Real-World Evidence studies and ensuring rigorous statistical analysis and reporting in a collaborative environment. Ideal candidates will possess an advanced degree in biostatistics, have at least 5 years of relevant experience, and be proficient in SAS programming. Benefits include flexible working arrangements and opportunities for professional growth.

Prestations

Flexible working arrangements

Exposure to international clients

Professional growth opportunities

Collaborative consulting environment

Qualifications

• 5+ years of experience as a Lead Biostatistician in a CRO, biotech, or pharmaceutical setting.
• Strong understanding of observational study design and analysis processes.
• Ability to present complex statistical concepts to diverse audiences.

Responsabilités

• Lead complex Real-World Evidence studies and provide statistical oversight.
• Develop and review Statistical Analysis Plans ensuring regulatory compliance.
• Act as a subject matter expert in statistical matters.

Connaissances

SAS programming

Statistical analysis

Project leadership

Communication skills

Attention to detail

Formation

Advanced degree in biostatistics or related field

Doctoral degree preferred

Outils

SAS

Description du poste

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Senior Biostatistics Manager in France.

This role sits at the center of advanced Real-World Evidence initiatives, supporting high-impact studies for leading pharmaceutical and biotech organizations. You will lead complex statistical programs, contribute to post-market and regulatory strategies, and ensure scientific rigor across study design, analysis, and reporting. Working within a collaborative consulting environment, you will partner closely with cross‑functional teams and senior stakeholders. The position combines hands‑on statistical expertise with strategic leadership and external visibility. Your work will directly influence regulatory decisions and scientific publications. This is an ideal opportunity for an experienced biostatistician looking to shape the future of evidence‑based healthcare.

Accountabilities

• Lead complex RWE studies and multi‑protocol programs, providing end‑to‑end statistical oversight and coordination across teams and locations.
• Develop and review complex Statistical Analysis Plans, ensuring methodological soundness and regulatory alignment.
• Perform senior‑level review of Tables, Figures, and Listings prior to client delivery.
• Contribute to protocol development by authoring statistical sections under senior statistical guidance.
• Act as a subject matter expert, supporting internal initiatives, procedural documentation, and best practices.
• Participate in bid defenses, client meetings, and strategic discussions as a statistical lead.
• Present insights and share knowledge internally and at external scientific conferences and forums.

Requirements

• Advanced degree in biostatistics, computer science, or a related field; a doctoral degree is strongly preferred.
• At least 5 years of experience as a Lead Biostatistician within a CRO, biotech, or pharmaceutical environment.
• Strong programming expertise in SAS, including non‑parametric methods, linear and non‑linear models, categorical data, and survival analysis.
• Proven experience working with SDTM and ADaM datasets, as well as producing high‑quality Tables, Figures, and Listings.
• Solid understanding of observational study design, analysis, and reporting processes.
• Demonstrated ability to clearly communicate complex statistical concepts to technical and non‑technical audiences.
• Strong organizational skills, attention to detail, and an autonomous yet collaborative working style.

Benefits

• Opportunity to work on high‑visibility, global Real‑World Evidence projects.
• Flexible working arrangements, including remote work options.
• Exposure to international clients, scientific publications, and regulatory‑driven studies.
• Collaborative consulting environment focused on innovation and scientific excellence.
• Professional growth through leadership opportunities and knowledge‑sharing platforms.

Why Apply Through Jobgether?

We use an AI‑powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top‑fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!

Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre‑contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.