Associate Director, Biostatistics

Beigene; France; À distance; EUR 60 000 - 100 000; Plein temps

Résumé du poste

An established industry player seeks an Associate Director of Biostatistics to lead statistical solutions for EU HTA requirements. This role involves collaborating with cross-functional teams, providing strategic input for evidence generation, and innovating data analysis methods. The ideal candidate will have a strong background in statistical methodologies, excellent communication skills, and a passion for improving cancer treatments. Join a dynamic team dedicated to making a difference in oncology and enjoy a supportive environment that fosters professional growth and collaboration.

Qualifications

• PhD or Master’s in Statistics/Biostatistics with relevant experience.
• Extensive experience with HTA in Europe and major markets.

Responsabilités

• Collaborate with teams to support HTA submissions in Europe.
• Build models for EU submissions focusing on HTA/JCA analysis.

Connaissances

Statistical Methodologies

HTA Knowledge

SAS

R

Communication Skills

Team Collaboration

Detail-oriented

Formation

PhD in Statistics/Biostatistics

Master’s in Statistics/Biostatistics

Description du poste

Associate Director, Biostatistics

Apply locations: France, Remote

Type: Full time

Posted: 2 Days Ago

Job Requisition ID: R27769

BeiGene, Ltd. has proposed to change its name to BeOne Medicines Ltd. The new name is subject to shareholder approval and, once approved, use of the name will be phased in over 2025. During this transition, both names may be used to describe the company. BeOne continues to grow rapidly and offers exciting opportunities for experienced professionals. We seek scientific and business professionals who are highly motivated, collaborative, and share our passion for fighting cancer.

General Description:

We are seeking a highly motivated, proactive, and strategic statistician with strong expertise in EU HTA methodologies. The role involves providing statistical solutions to meet EU HTA requirements, including the EU Joint Clinical Assessment (JCA), and helping shape organizational processes. The candidate will collaborate closely with functions such as HEOR, Market Access, Clinical Development, Regulatory, and Medical Affairs.

Essential Functions:

1. Collaborate with cross-functional teams to support HTA submissions in Europe.
2. Provide strategic statistical input for evidence generation and analysis for the EU JCA.
3. Support local HTA adaptations with quantitative analysis.
4. Help shape new organizational approaches to meet EU JCA needs.
5. Serve as a subject matter expert in EU cross-functional teams.

Responsibilities:

1. Build models supporting EU submissions, focusing on HTA/JCA analysis, in collaboration with HEOR and external vendors.
2. Attend advisory and strategic meetings, providing statistical analysis input.
3. Work with statistical programming staff to ensure compliance with analysis requirements.
4. Innovate data analysis methods, interpret results, and present findings to leadership.
5. Stay updated on statistical methodologies in HTA, including economic modeling and observational studies.
6. Identify and resolve technical or design issues in studies.
7. Act as statistical SME in cross-functional teams.
8. Contribute to training, SOPs, and departmental documentation.
9. Provide support for local adaptations and ad hoc HTA requests.
10. Ensure consistency and standards across compounds and areas.
11. Review vendor data and analyses as needed.

Qualifications:

• PhD in Statistics/Biostatistics or related field with ≥5 years' experience, or Master’s with ≥7 years' experience.
• Extensive experience with HTA in Europe and major markets.
• Strong knowledge of statistical methodologies and experimental design.
• Proficiency in SAS and R.
• Excellent communication skills in English.
• Proactive, detail-oriented, and motivated.
• Interest in statistical research and novel methods.
• Ability to work in a team with cross-functional members.
• Knowledge of clinical trial design and drug development processes.
• Experience in planning, analysis, and reporting of trials.

Travel: Yes, as needed.

Global Competencies:

We value behaviors aligned with our core values: Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit. These include fostering teamwork, providing honest feedback, self-awareness, inclusivity, initiative, entrepreneurial mindset, continuous learning, embracing change, results orientation, analytical thinking, financial excellence, and clarity in communication.

We are an equal opportunity employer committed to diversity and do not discriminate based on race, religion, gender, age, disability, or other protected categories. Employment decisions are based on qualifications, merit, and business needs.

About Us

BeiGene, Ltd. plans to change its name to BeOne Medicines Ltd., pending shareholder approval, with a phased transition in 2025. During this period, both names may be used.

BeOne is a global oncology company developing innovative, affordable cancer treatments. Our pipeline is advancing through internal efforts and collaborations. We are dedicated to improving access to medicines worldwide. Our team of over 11,000 colleagues spans six continents. To learn more, visit www.beigene.com and follow us on LinkedIn, X, Facebook, and Instagram.

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Our Values

How we work is as important as what we do. Our core values guide our decisions and actions.