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.
As a Senior Clinical Research Associate, you will monitor clinical trial sites, ensure adherence to protocols and regulatory standards, and collaborate with cross-functional teams to ensure data integrity and participant safety.
ICON offers competitive salary 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 monitoring experience
Clinical trial site monitoring
Good Clinical Practice (GCP) standards
Ability to travel 60% internationally and domestically
Site management and data integrity
Proficiency in clinical trial software
Nice-to-have
Strong organizational and problem-solving skills
Excellent communication and interpersonal skills
Stakeholder management and influence
Building effective site relationships
Providing training and guidance
Key Requirements
Advanced degree in life sciences, nursing, or medicine