Senior Clinical Research Associate (CRA)

About the role

ICON is seeking a Senior CRA to lead clinical trial monitoring within its sponsor‑dedicated model. You will ensure trials are conducted to protocol, regulatory and GCP standards while contributing to the development of life‑changing treatments.

Key responsibilities

• Monitor clinical trial sites for compliance with study protocols, regulatory requirements and Good Clinical Practice.
• Conduct site visits, assess performance, resolve issues and provide support to ensure successful trial execution.
• Collaborate with cross‑functional teams to guarantee timely and accurate data collection and reporting.
• Provide training and guidance to site staff and fellow CRAs to maintain high standards of conduct.
• Build and maintain effective relationships with site personnel and stakeholders.

Required profile

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

Required skills

• Clinical trial monitoring practices and site management.
• Data integrity assurance and use of clinical trial software/tools.
• Good Clinical Practice (GCP) knowledge.

What we offer

• Competitive base salary and performance‑related incentives.
• Health, dental and vision coverage where applicable.
• Retirement and pension plans, life assurance and disability coverage.
• Learning and development opportunities through structured training and career pathways.