You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively
Job Summary
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities.
At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.
Matching Summary
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Skills & Requirements
Must-have
Clinical trial monitoring experience
ICH-GCP guidelines knowledge
Protocol compliance
Data integrity
Patient safety
Nice-to-have
Inclusive environment
Fast-paced environment
Work-life balance opportunities
Collaborative team player
Key Requirements
Minimum of 2 years of experience as a Clinical Research Associate
Bachelor's degree in a scientific or healthcare-related field
Willingness to travel as required (approximately 60%)