Clinical Research Associate at ICON

Elevate your career as a Clinical Research Associate at ICON plc, a leader in healthcare intelligence. Monitor clinical studies with a focus on oncology, ensuring trials meet all regulatory standards.
As a Clinical Research Associate, you'll engage in monitoring clinical trials either onsite or remotely, ensuring compliance with protocols and regulatory requirements. A Bachelor's degree in a scientific field is necessary, along with at least 1 year of clinical monitoring experience for Level 2 roles. Your ability to travel up to 70% of the time will be essential for effective oversight of studies.
Key Responsibilities:
• Monitor clinical studies at investigative sites or remotely
• Ensure compliance with protocols, SOPs, and regulations
• Report study progress accurately and timely
• Collaborate with cross-functional teams on study objectives
• Assist in resolving study-related issues
Requirements:
• Bachelor's degree or equivalent in a scientific field
• ...