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  "job_description": "Les missions du poste\n\nExcelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.\n\nFounded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.\n\nWe take a one-team approach to work: our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.\n\nExcelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.\n\nExcelya is seeking a Statistical Programmer to join our innovative team dedicated to advancing clinical research. We pride ourselves on our core values of Audacity, Care, and Energy, and we believe that your expertise can help us make a significant impact in the healthcare domain.\n\nAs a Statistical Programmer, you will play a critical role in processing and analyzing clinical trial data. Utilizing your programming skills, you will ensure the accuracy and integrity of statistical outputs, contributing to the development of high-quality study reports.\n\nKey Responsibilities:\n\n- Develop, validate, and maintain SAS programs for clinical data analysis and reporting.\n- Generate statistical tables, listings, and graphics in accordance with study specifications.\n- Collaborate with biostatisticians and data management teams to clarify deliverables and timelines.\n- Conduct quality control checks on programming outputs to ensure data consistency and compliance with regulatory standards.\n- Provide documentation and support for all programming activities, including maintaining version control.\n- Assist in the preparation of statistical analysis plans and regulatory submissions as needed.\n\nLe profil recherché\n\nWhy Join Us?\n\nAt Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.\n\nHere's what makes us unique-\n\nWe are a young, ambitious health company representing 900 Excelyates, driven to become Europe'sleading mid-size CROwith thebest employee experience. Ourone-stop provider service model-offering full-service, functional service provider, and consulting-enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.\n\nExcelling with caremeans benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.\n\nQualifications\n\nTo thrive in this role, you should possess a unique combination of technical skills and statistical knowledge.\n\n- Experience: At least 2 years of experience in statistical programming, ideally within clinical trials.\n- Technical Skills: Strong proficiency in SAS; knowledge of R or Python is advantageous.\n- Education: Bachelor's degree in Statistics, Mathematics, Computer Science, or a related discipline.\n- Language Skills: Fluent in English, both written and spoken.\n- Soft Skills: Detail-oriented, strong analytical thinking, effective teamwork, and communication skills are essential.\n\nBienvenue chez Excelya\n\nExcelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.\n\nFounded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.\n\nWe take a one-team approach to work: our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.\n\nExcelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.",
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  "job_posted_at_timestamp": 1773187200,
  "job_posted_at_datetime_utc": "2026-03-11T00:00:00.000Z"
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