Overview

As a Senior CRA, you oversee clinical trial monitoring to ensure adherence to protocol, GCP, and regulatory standards. You operate within ICON’s sponsor-dedicated model and collaborate with cross-functional teams to support trial execution. You will train site staff, manage relationships with site personnel, and drive quality and continuous improvement. This role offers global exposure, a pathway for career development, and meaningful impact on patient outcomes.

Compensaciones / Incentivos

- Competitive base salary
- Health and wellbeing programmes
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities

Responsabilidades

- Monitor sites to ensure compliance with study protocols, GCP, and regulatory requirements
- Conduct site visits to assess performance, resolve issues, and support trial execution




- Collaborate with cross-functional teams to ensure timely data collection and reporting
- Provide training and guidance to site staff and fellow CRAs
- Build and maintain relationships with site personnel and stakeholders to facilitate smooth operations

Requisitos principales

- Bachelor in relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate
- Ability to manage multiple sites and projects simultaneously
- Expertise in monitoring practices, data integrity, and site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication and stakeholder management skills
- Willingness to travel approximately 60%

- communication
- stakeholder management
- problem-solving
- monitoring practices
- data integrity
- site management

📌 Senior Clinical Research Associate - barcelona
🏢 Icon Clinical
📍 Barcelona