You will support clinical trial sites by managing logistics, resolving site-related issues, and ensure that sites are equipped with the necessary resources to conduct trials effectively
Job Summary
You will support clinical trial sites by managing logistics, resolving site-related issues, and ensure that sites are equipped with the necessary resources to conduct trials effectively.
Key responsibilities include: Providing logistical and operational support to clinical trial sites, ensuring timely and efficient delivery of materials and supplies.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
Matching Summary
You will support clinical trial sites by managing logistics, resolving site-related issues, and ensure that sites are equipped with the necessary resources to conduct trials effectively.
Skills & Requirements
Must-have
Logistical and operational support
Resolve site-related issues
Ensure adherence to study protocols
Track site performance metrics
GCP and regulatory compliance
Nice-to-have
Foster an inclusive environment
Drive innovation and excellence
Shape the future of clinical development
Key Requirements
Bachelor's degree in a relevant field
Experience in site management or clinical operations preferred
Strong problem-solving and organizational skills
Knowledge of clinical trial processes, GCP, and regulatory requirements is a plus
Willingness to travel as required (approximately 1%)