Bachelor’s degree in health, clinical, biological, mathematical sciences, or related field, Minimum 5 years of direct Data Management experience, including 3+ years as a CDM project lead, Proven experience managing multiple global trials through the full data management lifecycle (large trials of 1000+ patients), Advanced knowledge of data management processes, including SAE reconciliation, vendor data integration, and emerging technologies, Strong understanding of GCP and relevant regulatory guidelines, Excellent communication, organizational, and project management skills, Ability to work independently and build effective relationships with clients and internal teams, Comprehensive knowledge of clinical drug development processes, Fluency in English, both written and spoken

sharing the costs of sports activities, private medical care, life insurance, remote work opportunities