Senior Clinical Research Associate (Unblinded)

About the role

ICON is a global healthcare intelligence and clinical research organisation seeking a Senior CRA to support unblinded clinical trials. The role focuses on ensuring trial activities meet protocol, regulatory and GCP standards while driving quality and compliance.

Key responsibilities

• Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conduct site visits to 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 guidance to site staff to maintain high standards of trial conduct.
• Build and maintain effective relationships with site personnel and stakeholders.

Required profile

• Bachelor's degree in a relevant scientific or healthcare discipline.
• At least 1 year of experience as a Clinical Research Associate on unblinded studies.
• Strong understanding of clinical trial processes, monitoring practices, and regulatory requirements.
• Proven ability to manage multiple sites simultaneously with strong organizational and problem‑solving skills.
• Excellent communication, interpersonal, and stakeholder management abilities.
• Oncology experience is highly desirable.
• Willingness to travel approximately 35%, including occasional travel within LATAM.

What we offer

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