ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence.
The role involves monitoring clinical trial sites, ensuring adherence to protocols and regulatory requirements, collaborating with cross-functional teams, and providing training and guidance to maintain high standards.
ICON offers competitive salaries and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.
Matching Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence.
Skills & Requirements
Must-have
Oncology clinical trial monitoring
Good Clinical Practice (GCP) compliance
Site performance assessment
Clinical trial software proficiency
Travel at least 60% internationally and domestically
Valid driver’s license
Multi-site and project management
Nice-to-have
Strong organizational skills
Problem-solving abilities
Excellent communication skills
Stakeholder management
Inclusive and diverse culture
Training and mentoring site staff
Key Requirements
Advanced degree in life sciences, nursing, or medicine