Descripción de la oferta
**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 communicationskills. + 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.* 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 **Pursue** *Progress*. **Discover** *Extraordinary*.Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together. 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.Watch our and check out our Diversity Equity and Inclusion actions at !#LI-Hybrid #BarcelonaHub #SanofiHubsDiversity und Inklusion sind in den Grundwerten von Sanofi verankert und spiegeln sich in unserer Arbeitsweise wider. Wir respektieren die Vielfalt unserer Belegschaft in Hinsicht auf ihre Herkunft, Erfahrungen und Lebensweisen. Wir erkennen die Bereicherung, die diese Vielfalt birgt, und fördern Inklusion sowie eine Arbeitsumgebung, in der diese Unterschiede sich weiter entwickeln können, zur Stärkung des Lebens unserer Mitarbeiter, Patienten und Kunden.**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.#J-18808-Ljbffr
