Opportunity Description
Manager, Study Start Up - Amsterdam area
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a **Manager, Study Start Up** at ICON, you will lead and oversee the start-up activities for clinical trials, ensuring that all processes are completed efficiently and in compliance with regulatory requirements.
**What You Will Do:**
You will manage day-to-day site start-up and activation activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
+ Coordinate and oversee the preparation, review, and approval of regulatory and ethics submissions at country and site level, ensuring compliance with ICH-GCP, local regulations, and ethical standards.
+ Monitor global regulatory and EC/IRB environments,...
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a **Manager, Study Start Up** at ICON, you will lead and oversee the start-up activities for clinical trials, ensuring that all processes are completed efficiently and in compliance with regulatory requirements.
**What You Will Do:**
You will manage day-to-day site start-up and activation activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
+ Coordinate and oversee the preparation, review, and approval of regulatory and ethics submissions at country and site level, ensuring compliance with ICH-GCP, local regulations, and ethical standards.
+ Monitor global regulatory and EC/IRB environments,...
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