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In this role, you drive site engagement to support efficient clinical trials and ensure compliant study conduct. You will collaborate with trial sites and internal teams to tailor engagement strategies, monitor performance, and foster strong, compliant relationships. The position offers impact across multiple studies and sites, contributing to ICON’s mission to bring new medicines to patients faster.
You will work in a values-driven environment that prioritizes integrity, collaboration, agility, and inclusion.
Compensaciones / Incentivos
- Build and maintain relationships with key trial-site stakeholders (PI, site coordinators, research staff)
- Provide guidance on study protocols, procedures, and regulatory requirements to site staff
- Identify opportunities to improve site engagement and optimize site performance
- Collaborate with internal teams to develop and implement site engagement strategies per study/site needs
- Monitor site performance metrics and report engagement outcomes to study teams
- Support delivery of clinical research activities with accountability for deliverables
Responsabilidades
- Bachelor's degree in life sciences or related field
- Previous experience in clinical research, site management, or related field (preferred)
- Strong interpersonal and communication skills to build rapport with diverse stakeholders
- Excellent organizational and problem-solving abilities with multitasking xugodme capacity
- Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials
- Willingness to travel approximately 60%
- Eligibility to work legally in the country of the role
Requisitos principales
- Competitive base salary
- Performance-related incentives
- Health and wellbeing programmes (medical, dental, vision)
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
📌 Site Engagment Liason (Barcelona)
🏢 Icon Clinical
📍 Barcelona
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