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
Job Summary
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.
You will manage day-to-day site start-up and activation activities, supporting your team to deliver quality outcomes.
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 lead and oversee the start-up activities for clinical trials, ensuring that all processes are completed efficiently and in compliance with regulatory requirements.
Skills & Requirements
Must-have
End-to-end study start-up process
Site identification and feasibility
Regulatory submissions and site activation
Global regulatory requirements
Clinical operations understanding
Process optimization and best practices
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Team guidance and mentorship
Continuous improvement initiatives
Key Requirements
Bachelor's degree in relevant scientific or healthcare field
Extensive clinical trial study start-up experience
Proven leadership and team management skills
Excellent organizational and project management skills
Strong communication and stakeholder management skills