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
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, clinical operations, or a related field is 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%)