Senior Biostatistician - Patient Reported Outcomes (M/F)

TN France; France; Sur place; EUR 60 000 - 100 000; Plein temps

Résumé du poste

Join a leading global healthcare consulting firm as a Senior Biostatistician, where your expertise in R Programming and statistical analysis will help shape patient-centric studies. This role offers the opportunity to lead biostatistics activities, manage client relationships, and mentor junior team members in a dynamic and collaborative environment. With a focus on innovative study designs and real-world evidence projects, you'll play a crucial role in improving global access to medicines. If you're passionate about making a difference in healthcare and thrive in a fast-paced team, this is the perfect opportunity for you.

Qualifications

• 5-8 years of experience in bio/pharma/CRO.
• Fluency in English and strong communication skills.

Responsabilités

• Lead biostatistics activities and manage client relationships.
• Analyze data, interpret results, and present findings to clients.

Connaissances

R Programming

Statistical Analysis

SQL

Communication Skills

Client Relationship Management

Formation

MSc in Statistics

PhD in Biostatistics

Outils

STATA

Statistical Software

Description du poste

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Client:

Oracle

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Job Category:

-

EU work permit required:

Yes

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Job Reference:

17f394a392c0

Job Views:

1

Posted:

24.04.2025

Expiry Date:

08.06.2025

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Job Description:

Oracle Life Sciences is a leading global healthcare consulting firm and trusted advisor to many of the world’s top pharmaceutical, biotech, and medical device & diagnostic companies. We support the work of Oracle Life Sciences by working with healthcare companies to improve global access to medicines through science and research. We are passionate about our people, our business, and our clients, fostering a culture that contributes to health and well-being.

With ongoing developments in Oncology and Rare Diseases, a focus on targeted medicine, and integration of technology into medicine development and delivery, now is an exciting time to work in Life Sciences. Join us to make a difference in our clients' and patients' lives.

Due to growth, Oracle Life Sciences seeks a talented Senior Biostatistician with R Programming skills and knowledge of Patient Studies / PRO for Real-World Evidence projects.

You will be key in developing patient-centric studies, including Epi. Studies, Preference Studies, Patient Reported Outcomes surveys, Burden / Quality of Life studies, Physician surveys, and Chart reviews.

As a Senior Biostatistician, you will handle all statistical aspects of projects, including design, analysis, and proposal contributions. Your expertise will enable you to research, advise, and implement innovative designs for complex studies, ensuring high-quality, fit-for-purpose statistical solutions for clients.

Join a passionate team in an open environment, working on diverse topics and developing your skills alongside experts.

MISSION

1. Be the Subject Matter Expert (SME) for biostatistics and client discussions;
2. Understand client business issues;
3. Manage client relationships on Biostats matters throughout projects;
4. Lead biostatistics activities within the team;
5. Contribute to proposals with statistical inputs, including sample size calculations, and participate in bid defenses;
6. Serve as the primary contact for the study team on biostatistics questions;
7. Develop and review statistical sections of protocols, analysis plans, and deliverables;
8. Analyze data, interpret results, and provide recommendations;
9. Present results to clients;
10. Supervise and mentor junior team members;
11. Provide training on statistical methods;
12. Adopt new analytical methodologies to meet research needs.

QUALIFICATION

• MSc or PhD in Statistics, Biostatistics, or related field;
• 5-8 years of relevant experience in bio/pharma/CRO;
• Fluency in English (C2);
• Proficiency in R and STATA;
• Knowledge of programming logic, SQL, and macro programming;
• Deep understanding of study designs and statistical analysis;
• Strong communication skills for client interactions;
• Ability to work effectively in a fast-paced team environment;
• Experience in Preference studies and PRO development/validation is a plus;
• Knowledge of clinical trial methodologies and regulatory expectations is a plus.