Make a real impact on patients’ lives by powering high-quality, compliant clinical trials across a multi-country cluster
Job Summary
Make a real impact on patients’ lives by powering high-quality, compliant clinical trials across a multi-country cluster.
You’ll be the central connector for Clinical Operations Managers, Clinical Research Managers, Clinical Research Associates, and study sites across multiple countries.
We offer a dynamic and international work environment where you will have the opportunity to grow and develop your skills while contributing to meaningful research.
Matching Summary
Make a real impact on patients’ lives by powering high-quality, compliant clinical trials across a multi-country cluster.
Skills & Requirements
Must-have
Clinical Trial Management Systems (CTMS)
Regulatory compliance including ICH-GCP
Clinical trial documentation management
Site readiness coordination
Cross-functional team collaboration
Nice-to-have
Tech-savvy and detail-driven
Positive mindset and resilience
Continuous improvement mindset
Multicultural global team experience
Strong communication and negotiation skills
Key Requirements
Bachelor’s degree preferred in life sciences or health-related field
Experience in clinical research environment
Knowledge of ICH-GCP and Good Documentation Practices