Participates in internal communication of results,. Establishes effective communication with various internal stakeholders to understand and support the……
Ensure achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and……
Ensures achievement of the start-up and clinical deliverable within the contractual time period specified by preparing and monitoring start-up and clinical……
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and……
Design, implementation and coordination of clinical studies with the support of Clinical Operations, Pharmacovigilance, Biometrics and Medical Writing:…
Vous rejoindrez l’équipe Contrôle Qualité des réactifs d’immunodosages automatisés et contribuerez à garantir la qualité, la conformité et la fiabilité de nos……
The Quality Manager ensures the compliance, performance, and continuous improvement of the quality management system in order to guarantee customer satisfaction……
Excellent communication skills (written and verbal). In this role, you will work under the direction of the Team Lead or Project Manager and be responsible for……
Develop post-market evidence plans: PMCF, AI life cycle management. Main Mission: To design and deliver the clinical real-world evidence needed to gain……
Nous nous engageons à créer un lieu de travail où chacun se sent écouté, valorisé et soutenu, où nous incarnons « The Real Us*». Drive Vision and Strategy (2).…
5 years of management experience. 5 years of experience in regulatory bioanalysis (CRO or pharmaceutical industry), including immunogenicity testing and large……
5 to 8 years in a similar position with experience in similar products and similar markets. Strong technical analysis and communication skills.…
Au sein d’une startup de la medtech early qui développe un dispositif médical implantable dédié à traiter le diabète de type II. PHD en chimie ou en Biologie.…
Vous êtes rigoureux(se) et vous possédez l'esprit d'équipe. Rédiger tout ou partie des dossiers et participer au transfert technique en production.…
This position requires excellent relationship management, teamwork, and strategic planning. Responsible for understanding and satisfying the requirements for……
Etre force de proposition sur les sujets liés à son activité et l’amélioration de sa performance. Nous aidons nos clients à garantir la qualité et l’innocuité……
100% employer-covered health insurance, On-site restaurant, Works council (CSE) benefits. Serve as Lead Study Director for multi-site studies when required.…
This position sits at the intersection of Business Development, R&D, Regulatory, Medical, and Commercial, ensuring seamless execution from asset assessment……
Male of female with Ph.D. in Statistics with minimum 3 years of relevant pharmaceutical (or CRO) industry work experience or Masters in Statistics or equivalent……
Ability to partner with cross-functional teams at the site and globally to support Fillers New Product Development initiatives and drive the Quality Culture at……
You will be involved in developing, optimizing, and implementing IHC and ISH assays on automated platforms (5 Ventana Discovery instruments), combined or not……
Établir et maintenir des relations solides avec les KOLs pour obtenir un retour d'expert (feedback) sur le design produit, soutenir les études cliniques et……
This position requires excellent relationship management, teamwork, and strategic planning. Responsible for understanding and satisfying the requirements for……
Strong project coordination, communication, and stakeholder management skills. Catalent est un employeur garantissant l'égalité des chances et ne fait aucune……
Use AI to find out how well the skills on your resume fit this job description.
Date de parution: 30 juin 2026
Ville: Gif-sur-Yvertte
Pays/Région: FR
Type de contrat: CDI
N° offre: 11945
Senior Real World Evidence Statistician (H/F)
Nous sommes un groupe pharmaceutique à dimension humaine, international et indépendant, gouverné par une Fondation. Notre modèle, singulier, fait notre fierté mais, surtout, nous permet de servir pleinement notre vocation : « Engagés pour le progrès thérapeutique au bénéfice des patients ».
Aujourd’hui leader mondial en cardiologie, nous avons choisi de devenir un acteur focalisé et innovant en oncologie d’ici 2030, en ciblant des cancers difficiles à traiter et en y consacrant plus de 70 % de notre budget R&D. Un défi que nous poursuivons en parallèle du développement de notre activité générique pour un accès à des soins de qualité pour tous, et à moindre coût.
Nous ? 22 000 passionnés de plus de 50 nationalités, portés par un esprit d’entreprenariat. Chaque jour nous avançons avec et pour les patients, avec et pour nos équipes, portés par l’envie de prendre soin, d’oser, de nous développer, de nous engager pour être utiles à celles et ceux qui en ont besoin.
Venez vivre et contribuez à faire vivre notre engagement #MovedByYou
www.servier.com
As a senior RWE statistician, you join an international and committed team, in charge of methodological and statistical approaches serving our real-world data studies and supporting related development plans.
You drive the RWD studies you are assigned, ensuring state-of-the-art methodologies and deliverables, in compliance with regulatory guidelines as well as all Servier policies and procedures.
Main responsibilities: Collaborates in the preparation of the RWD study protocol: methodological choices, statistical estimation of the number of patients and statistical analysis strategy.
Develop, implement or advise on appropriate new statistical methodologies and keep abreast of current issues and developments in statistical innovation with RWE applications.
Ensures RWE data statistical analysis:
Contributes to statistical methodology definition for study designs
Writes the Statistical Analysis Plan (SAP), the table/listings/graph document (TLG),
Perform data analyses for real-world datasets
Ensures validation of the results produced and their validity and robustness,
Participates in internal communication of results,
Review the study report and ensures proper statistical interpretation of the results
Collaborates with multi-disciplinary project teams to establish project goals and timelines.
Establishes effective communication with various internal stakeholders to understand and support the strategy for when and how to use RWD.
Contributes to productive collaborations with other stakeholders, promoting teamwork, quality, operational efficiency and innovation
Lead or participates in working groups on methodological and statistical issues, as well as in transversal and multidisciplinary projects
Contributes to the internal and external visibility of the department and promote the development of internal scientific knowledge.
Profile :
Master or Doctoral degree or equivalents in Biostatistics, Statistics or closely related fileds.
5 years’ experience as statistician for real-world data studies
Strong knowledge of real-world study methodologies
Experience leading secondary data analysis, including medical claims, electronic medical records, chart reviews, and registries.
Mastery of regulatory guidelines (FDA, EMEA, ICH)
R expertise
Ability to effectively communicate with others on the project team and in the department; strong interpersonal communication skills
Detail oriented, well organized with the ability to work on several projects simultaneously
Excellent team player, collaborative and maintains a positive, results-orientated work environment
English fluency is required
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.