AI-powered risk and data quality oversight for clinical trials
CluePoints builds AI-driven risk assessment and data quality software for clinical trial operators, grounded in Python, Java, and ML (TensorFlow, PyTorch) running on Azure and Kubernetes. The stack reveals a data-heavy, infrastructure-conscious engineering organization — they're actively investing in CI/CD templating, developer infrastructure, and data pipeline optimization, indicating maturation beyond initial product-market fit. Hiring velocity has slowed but remains focused on engineering and senior talent, with notable gaps in leadership around revenue scaling (sales and commercial roles represent smaller cohorts).
Notable leadership hires: Chief of Staff, Key Account Director
CluePoints operates in regulated clinical trial oversight, providing software that applies statistical monitoring and machine learning to detect quality and integrity issues in trial data during and after studies. The product is designed to align with FDA, EMA, ICH, and MHRA guidance and covers central monitoring, on-site monitoring, and medical review workflows. Founded in 2012, the company operates from Belgium with a 201–500-person team distributed across Belgium, the UK, US, and Poland. Current priorities include scaling data pipeline capacity, expanding enterprise customer relationships, and improving trial operational efficiency within a risk-based monitoring framework.
CluePoints builds on Python, Java, C#, and C++ with ML frameworks (TensorFlow, PyTorch). Infrastructure runs on Azure (Kubernetes, Web Application Firewall) with MySQL, MongoDB, and Databricks for data. Message queues include RabbitMQ and ZeroMQ.
Headquartered in Louvain-La-Neuve, Belgium. Currently hiring across Belgium, United Kingdom, United States, and Poland, with 41 active roles focused on engineering (13 open), support (7), and sales (5).
Risk-based quality management (RBQM) and data quality oversight for clinical trials. Core areas include central statistical monitoring, risk monitoring, and data integrity assurance aligned with regulatory guidance from FDA, EMA, ICH, and MHRA.
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