As a Clinical Data Coordinator at ICON, you will be responsible for overseeing the collection, management, and quality of clinical data to ensure compliance with regulatory requirements and project timelines
Job Summary
As a Clinical Data Coordinator at ICON, you will be responsible for overseeing the collection, management, and quality of clinical data to ensure compliance with regulatory requirements and project timelines.
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.
At ICON, inclusion & belonging are fundamental to our culture and values, and the company is dedicated to providing an inclusive and accessible environment for all candidates.
Matching Summary
As a Clinical Data Coordinator at ICON, you will be responsible for overseeing the collection, management, and quality of clinical data to ensure compliance with regulatory requirements and project timelines.
Skills & Requirements
Must-have
clinical trial data management
data entry and quality control
collaboration with cross-functional teams
proficiency in clinical trial management software
homebased midshift schedule
Nice-to-have
strong analytical skills
attention to detail
effective communication skills
commitment to quality and compliance
knowledge of industry trends and best practices
Key Requirements
Bachelor's degree in life sciences or related field