About this role

Support study start-up activities (feasibility, site selection, regulatory submissions)
Assist in building and maintaining study timelines and plans
Coordinate investigator meetings and support site activation
Oversee day-to-day trial operations across sites/countries
Ensure compliance with ICH-GCP and regulatory requirements
Monitor study progress, enrollment, and data quality
Identify risks and escalate as needed
Ensure audit/inspection readiness and quality standards
Review clinical data and support reporting to sponsors
Contribute to study reports and documentation

Opportunities for personal and professional growth in a rewarding environment
Team that values collaboration, quality, and making a difference in the lives of patients

Clinical Trial Manager – Freelance

Key skills