The Study Start-up/Site Activation Lead is responsible for managing start-up activities in compliance with client procedures and international guidelines such as ICH-GCP
Job Summary
The Study Start-up/Site Activation Lead is responsible for managing start-up activities in compliance with client procedures and international guidelines such as ICH-GCP.
ICON offers a diverse culture that rewards high performance and provides competitive benefits focused on well-being and work-life balance.
ICON is committed to providing an inclusive and accessible environment and ensures equal consideration for employment without discrimination.
Matching Summary
The Study Start-up/Site Activation Lead is responsible for managing start-up activities in compliance with client procedures and international guidelines such as ICH-GCP.
Skills & Requirements
Must-have
Clinical study start-up management
Regulatory submission processes
Site regulatory documentation management
ICH-GCP compliance
Project management skills
Study start-up milestone tracking
Nice-to-have
Excellent written and verbal communication
Ability to manage multiple priorities
Collaboration with local study teams
Supportive of inclusive work culture
Key Requirements
Bachelor’s Degree in life sciences
Minimum 5 years clinical research start-up experience
Strong understanding of regulatory and submission processes