Senior Clinical Research Associate

About the role

ICON is seeking a Senior Clinical Research Associate to lead monitoring activities for sponsor‑dedicated clinical trials. You will ensure trials are conducted according to protocol, regulatory requirements, and Good Clinical Practice 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, accurate data collection and reporting.
• Provide training and guidance to site staff and fellow CRAs to maintain high standards.
• 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 clinical 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

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

What we offer

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