Senior Biostatistician F - M H / F

Servier; Saclay; Sur place; EUR 65 000 - 85 000; Plein temps

Résumé du poste

A leading pharmaceutical company in France is seeking a Senior Biostatistician to join their international team. The role involves designing and analyzing clinical studies, with a focus on regulatory submissions (EMA, FDA). Candidates should have a Master's or PhD in Biostatistics or a related field, along with 6-8 years of experience in clinical statistics. Strong skills in SAS and R are required, and oncology experience is preferred. The position offers a supportive work environment and excellent benefits, including paid vacation and health insurance.

Prestations

23 RTT days

27 paid vacation days

8 telecommuting days per month

Performance-related bonus

Subsidized restaurant

Premium health insurance

Access to gym facilities

Qualifications

• 6-8 years' experience in clinical statistics with submission experience (EMA / FDA).
• Oncology experience preferred, but not required.
• Strong knowledge of ICH, EMA, and FDA guidelines.

Responsabilités

• Lead statistical strategy and deliverables for global clinical studies.
• Contribute to protocol design, SAPs, and clinical study reports.
• Support regulatory submissions and agency interactions.

Connaissances

Statistical strategy

Clinical statistics

Fluent English

Teamwork

Organizational skills

Formation

Master's or PhD in Biostatistics or Statistics

Outils

SAS

R

Description du poste

Long Description

Senior Biostatistician - Clinical Development (Oncology Preferred)

Join our international Biostatistics team dedicated to advancing innovative clinical programs. As a Senior Biostatistician, you'll play a key role in the design, analysis, and interpretation of clinical studies - driving projects from early development to regulatory submissions (EMA, FDA).

What you’ll do

• Lead statistical strategy and deliverables for global clinical studies.
• Contribute to protocol design, SAPs, and clinical study reports.
• Support regulatory submissions and agency interactions (EMA, FDA).
• Apply innovative methodologies, including modelling and simulation, to optimize study designs.
• Collaborate cross-functionally to ensure quality, efficiency, and scientific excellence.

What you bring

• Master's or PhD in Biostatistics, Statistics, or a related field.
• 6-8 years' experience in clinical statistics with submission experience (EMA / FDA).
• Oncology experience preferred, but not required.
• Strong expertise in SAS and R; solid knowledge of ICH, EMA, and FDA guidelines.
• Excellent communication, teamwork, and organizational skills.
• Fluent English (written & spoken).

What we offer

Within our Group, we strive to provide a stimulating and fulfilling work environment :

• Supportive, expert, and collaborative teams.
• Modern facilities and high-quality workspaces.
• 23 RTT days + 27 days of paid vacation per year.
• 8 telecommuting days per month.
• Exceptional leave for personal events and family milestones.
• Performance-related bonus, profit-sharing, and employee savings plan.
• Subsidized restaurant and premium health insurance (50% funded by the company).
• Various employee perks : vouchers, cultural and sports discounts, childcare support, and more.
• Access to gym facilities on certain sites.
• Proudly certified Top Employer (France & Europe) for three consecutive years.

Be part of a collaborative team shaping the future of innovative therapies through science and excellence.

Nous sommes engagés pour l'égalité des chances et le développement des talents dans toute leur diversité. Nous accordons autant de valeur à l'expérience qu'à l'envie de s'engager au quotidien pour être utile au progrès thérapeutique au bénéfice des patients. Si vous vous reconnaissez dans cette offre et ces quelques lignes, saisissez cette opportunité de nous rencontrer.