Overview
Join ICON as a Site Engagement Liaison to strengthen relationships with clinical trial sites and support compliant, efficient study conduct. You’ll work with investigators, site staff, and internal teams to tailor engagement strategies, monitor performance, and drive site-level impact. This role sits at the intersection of site operations and regulatory quality, enabling faster access to innovative therapies. You will thrive in a collaborative, value‑driven environment and travel as needed to sites.
Leistungen / Benefits
- Competitive base salary
- Health and wellbeing programmes
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes
- Learning and development opportunities
Verantwortungsbereiche
- Build and maintain relationships with stakeholders at clinical trial sites (PI, site coordinators, research staff)
- Provide guidance on study protocols, procedures, and regulatory requirements to ensure compliance
- Identify opportunities to improve site engagement and optimize site performance through feedback mechanisms
- Collaborate with internal teams to develop and implement site engagement strategies per study/site needs
- Monitor site performance metrics and report updates to study teams on engagement activities and outcomes
Zentrale Anforderungen
- Bachelor's degree in life sciences or related field
- Previous clinical research, site management, or related experience (preferred)
- Strong interpersonal and communication skills for diverse stakeholders
- Excellent organizational and problem-solving abilities with multitasking capacity
- Knowledge of ICH-GCP guidelines and regulatory requirements
- Willingness to travel approximately 60%
- Employment eligibility to work in country of role
- Interpersonal skills
- Communication
- Rapport-building
- Organizational skills
- Knowledge of ICH-GCP guidelines
- Clinical research / site management experience
Clinical Research Lead in Wiesbaden Arbeitgeber: Icon Clinical PLC
ICON ist ein hervorragender Arbeitgeber, der Ihnen die Möglichkeit bietet, in einem globalen Team von Fachleuten zu arbeiten, das sich leidenschaftlich für die Entwicklung neuer Medikamente einsetzt. Mit einem starken Fokus auf Zusammenarbeit, Innovation und kontinuierliche Weiterbildung fördert ICON eine inklusive Arbeitskultur, in der Ihre Fähigkeiten geschätzt werden und Sie aktiv zur Verbesserung der Arzneimittelentwicklung beitragen können. Darüber hinaus profitieren Sie von einem wettbewerbsfähigen Vergütungspaket und umfassenden Gesundheits- und Wellnessprogrammen, die auf Ihre berufliche und persönliche Entwicklung ausgerichtet sind.
