Clinical Statistics Team Lead

Sanofi US; Barcelona; Presencial; EUR 70.000 - 90.000; Jornada completa

Descripción de la vacante

A global healthcare company in Barcelona is seeking a Clinical Statistics Team Lead to oversee statistical support in clinical studies, ensuring quality deliverables. The ideal candidate has at least 7 years of experience in the pharmaceutical industry and is proficient in advanced statistical analyses using SAS and R. This role offers a supportive environment with opportunities for career growth and development.

Servicios

High-quality healthcare

Parental leave of at least 14 weeks

Wellbeing benefits

Formación

• 7+ years (MS) or 5+ years (PhD) pharmaceutical industry experience.
• Experience in project management preferred.
• Effective English communication skills required.

Responsabilidades

• Support clinical development plans and study design.
• Oversee statistical analyses and ensure quality control.
• Plan and track project activities and define team goals.

Conocimientos

Advanced statistical concepts

Project/study management

Interpersonal skills

SAS programming

R programming

Educación

MS or PhD degree in Statistics or relevant fields

Descripción del empleo

Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. Build a career and you can be part of transforming our business while helping to change millions of lives. Ready? As a Clinical Statistics Team Lead within our R&D Statistics Team at Barcelona, you’ll direct/oversee statistical support of a team of senior and principal biostatisticians, be accountable for statistical aspects and deliverables of the team and responsible for appropriate resource planning and allocation.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main responsibilities:

• Support the clinical development plan (CDP), the clinical study design (including protocol development), study setup and conduct.
• Oversee the execution of the statistical analyses according to the SAP and ISAP, prepare statistical methods & provide statistical insight into interpretation and discussion of results sections for the clinical study report (CSR) and/or publications to ensure the statistical integrity of the content according to internal standards and regulatory guidelines and in compliance with SOPs.
• Accountable for all assigned statistical deliverables related to one study or specific domain: statistical sections in protocol including sample size calculation, randomization specifications, and statistical methodology etc., SAP, data surveillance, statistical analysis results for CSR and its appendices (TLGs and in-text tables) …
• Propose, prepare and perform exploratory data analyses, ad-hoc analyses as relevant for the study or project objectives. Contribute to define and review the specific deliverables related to Transparency and Disclosure. Oversee the study data specifications, the production of the statistical analyses and the quality control coordinating with the programming team lead.
• Plan and track project/study activities and timelines. Contribute to operation process optimization and provide inputs to statistics and quality standards. Define team priorities and goals, conduct performance review and assist in problem solving. Define the development plan and conduct the continuous trainings for junior staff.
• Ensure productive collaborations with other functions in the aligned study team and/or safety monitoring team and in communicating with senior leadership.; Promoting teamwork, quality, operational efficiency, and innovation. Represent statistics to participate in scientific or technology working groups or cross function initiatives

About you

• Experience: 7+ years (MS) or 5+ years (PhD) of solid pharmaceutical industry experiences. Experience of project/with people management and development preferred.
• Soft and technical skills: Broad knowledge and good understanding of advanced statistical concepts and techniques, demonstrated strong project/study management, interpersonal and communication skills, good knowledge of pharmaceutical clinical development, together with early, late phase and post-marketing experiences, extensive ability to apply advanced statistical analyses using SAS and R languages, knowledge or experience with Artificial intelligence or Generative AI is a plus
• Education: MS or PhD degree in Statistics or relevant fields
• Languages: Highly effective communication in English, both oral and written.

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
• Build, develop and manage a statistics team support multiple TAs and different clinical phases
• Develop a career of being an influential statistician
• Gain international clinical trial experiences and communicate with Health Authorities worldwide

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.