Senior Clinical Research Associate

About the role

ICON plc is seeking a Senior Clinical Research Associate to lead monitoring activities for clinical trials. This remote position supports the delivery of high‑quality data while ensuring compliance with protocol, regulatory requirements, and Good Clinical Practice (GCP) standards.

Key responsibilities

• Monitor clinical trial sites to verify adherence to study protocols, regulatory requirements, and GCP standards.
• Conduct site visits, assess 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 fellow CRAs to maintain high standards of trial conduct.
• Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth operations.

Required profile

• Bachelor's degree in a scientific or healthcare‑related discipline.
• Extensive experience as a Clinical Research Associate with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects simultaneously.
• Strong organizational, problem‑solving, and communication skills.
• Willingness to travel up to 60% of the time.

Required skills

• Good Clinical Practice (GCP) knowledge.
• Proficiency with clinical trial software and tools.

What we offer

• Competitive salary package.
• Various annual leave entitlements.
• Health insurance options for you and your family.
• Retirement planning benefits.
• Global Employee Assistance Programme (LifeWorks) providing 24‑hour support.