Clinical trial services and CRO for pharmaceutical development
Aixial Group operates as a clinical development partner delivering end-to-end trial services, functional outsourcing, and consulting to pharmaceutical companies. The tech stack—Veeva Vault (RIM, Clinical, and vault infrastructure), CDISC standards, SAS, R, and Business Objects—reflects a regulated, data-heavy operation focused on trial design and regulatory submission. Active hiring in research and data roles across France, Bulgaria, and the US signals capacity expansion, while pain points around data governance, legacy data management, and EMA/FDA submission workflows indicate ongoing challenges in standardizing data flows across multi-project environments.
Aixial Group is a specialized clinical development partner serving pharmaceutical and biotech clients across trial design, execution, and regulatory strategy. The company operates through multiple service models: end-to-end trial delivery, functional service provider (FSP) arrangements, business process outsourcing (BPO), and expert consulting. Core capabilities span biometrics, biostatistics, medical writing, HEOR, data management, e-CRF systems, and SAS/R programming. Active projects include regulatory strategy, statistical analysis plan development, CMC (Chemistry, Manufacturing, and Controls) dossier management, and submission workflow optimization across EMA, FDA, and NMPA jurisdictions. The organization is headquartered in France and operates across multiple countries.
Veeva Vault (RIM, Clinical, and vault components), CDISC standards (SDTM), SAS, R, SQL, Git, Business Objects, Power BI, and Excel. This stack supports trial design, data management, biometrics, and regulatory submission workflows.
End-to-end clinical trial services, functional service provider (FSP) model, business process outsourcing (BPO), expert consulting, and staffing/resourcing. Specialties include trial design, biostatistics, medical writing, HEOR, and regulatory strategy.
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