Clinical Research Associate

About This Role

Join ICON plc's dynamic team as a Clinical Research Associate, overseeing and managing clinical trial activities in ophthalmology. Ensure compliance with protocols, regulations, and industry standards to maintain data integrity and participant safety.

Responsibilities

• Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
• Conduct site visits to assess site performance, resolve issues, and provide support for successful trial execution
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
• Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
• Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations

Requirements

• Extensive experience as a Clinical Research Associate
• Strong understanding of clinical trial processes and regulatory requirements
• Proven ability to manage multiple sites and projects simultaneously
• Strong organizational and problem-solving skills
• Expertise in monitoring practices, data integrity, and site management
• Proficiency in relevant clinical trial software and tools
• Excellent communication, interpersonal, and stakeholder management skills
• Ability to travel at least 60% of the time (international and domestic - fly and drive)
• Valid driver’s license

Qualifications

• Advanced degree in a relevant field such as life sciences, nursing, or medicine highly preferred
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.

Skills

* Required skills