Clinical trial CRO with regulatory, digital, and execution services across North America and Europe
Meditrial operates a contract research organization managing the full clinical trial lifecycle—from regulatory submissions through trial execution and digital tooling. The tech stack is PHP/MySQL/Angular-based, suggesting a legacy-forward engineering posture focused on maintaining existing trial management and regulatory systems rather than greenfield product builds. Hiring is heavily weighted toward research and healthcare roles (10 and 8 respectively) with senior-level concentration, reflecting a professional-services model where domain expertise and regulatory knowledge matter more than engineering headcount.
Meditrial is a clinical research organization founded in 2008, headquartered in New York with offices in Zürich, Berlin, Rome, London, and expanding into Latin America and Australia. The company provides end-to-end services across FDA approvals, IDE clinical trials, 510(k) submissions, EU and UK regulatory representation, and early feasibility studies. Core capabilities span clinical trial design and execution, regulatory document management, site selection, study budgeting, and digital health platforms. The business operates across 51–200 employees with steady hiring across research, healthcare, and clinical functions.
Meditrial actively hires across the United States, Italy, Germany, United Kingdom, Brazil, Peru, and Australia—reflecting its multi-office footprint and geographic expansion.
The stack centers on PHP, MySQL, and Angular, supplemented by Java, WordPress, and Git. This foundation supports regulatory documentation, study budgeting, trial master file setup, and enrollment management systems.
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