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 operational heartbeat of our studies—keeping sites moving, documents inspection-ready, and ensuring study files and systems are up to date.
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)
Electronic Trial Master Files (eTMF)
Regulatory compliance including ICH-GCP
Clinical trial documentation management
Multi-country clinical trial coordination
Nice-to-have
Cross-functional multicultural teamwork
Process simplification and continuous improvement
Strong communication and negotiation skills
Growth mindset and knowledge sharing
Digital tool proficiency
Key Requirements
Bachelor’s degree preferred in life sciences or related field
Experience in clinical research environment
Knowledge of ICH-GCP and Good Documentation Practices