Excelya is an independent clinical research partner founded in 2014 that delivers end‑to‑end CRO, FSP, and resourcing services to biotech, pharma, and medical‑device companies worldwide. With a global footprint spanning 28 countries and a team of over 900 specialists, the company offers integrated solutions in clinical operations, regulatory affairs, biostatistics, medical writing, pharmacovigilance, and data management. Its therapeutic focus includes oncology & hematology, rare disease & pediatrics, infectious diseases, immuno‑oncology, pain & CNS, and late‑phase/real‑world evidence studies. Excelya differentiates itself through a patient‑centered, excellence‑driven culture that blends compassionate care with rigorous scientific expertise to create bespoke, robust trial programs.
Open Positions
Chef de Projet Qualification/Validation
Engineering degree, experience in qualification/validation with project management, knowledge in qualification and aseptic process
Demand Planning Specialist
Master's degree, 0-2 years of experience, French and English proficiency
Clinical Research Associate Oncology
Proven ability to thrive in collaborative, fast-moving environments. Strong organizational abilities, problem-solving mindset, and excellent communication skills
Contract Specialist
Solid experience in Legal, Negotiation and/or Finance, strong organizational and communication skills, and proficiency in common software packages
Clinical Scientist Rare Disease
Support the Study Medical Manager, contribute to trial-related documents, and maintain medical and scientific documents
International PV Project Manager
Master's degree in Life Sciences, Fluent in written and spoken English and French, Solid understanding of global pharmacovigilance systems and regulatory requirements
International Clinical Operations Lead
Proven experience in managing international clinical operations, Master's degree in a relevant field, and fluency in French and English
Sterilization expert
2+ years experience, degree in Quality Assurance, Pharmacy, Process Engineering, or related field, fluency in French & English
Study Coordinator (ARC Hospitalier)
Bachelor's degree in Biology, Biochemistry, Pharmacology, Nursing, or a related field. Familiar with clinical trial regulations, ethics, data collection, patient follow-up, and documentation. Fluent in French and English
Senior Development Scientist - Project Leader
PhD in Biochemistry, Chemistry, Molecular Biology, Pharmacology, or related field, and 0-10 years of experience in R&D, specifically in biotransformation
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