Overview
As a Senior Clinical Research Associate at ICON plc, you oversee and manage trial activities to ensure protocol adherence, regulatory compliance, and data integrity. You will monitor sites, conduct visits, and collaborate with cross-functional teams to enable timely, compliant trial execution. You will train site staff and build strong site relationships to support successful studies. This role offers influence over trial quality, safety, and overall delivery within a globally respected CRO culture.
Leistungen / Benefits
- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- Global Employee Assistance Programme (EAP)
- Life assurance
- Flexible country-specific optional benefits
Verantwortungsbereiche
- Monitor clinical trial sites for protocol, regulatory, and GCP adherence
- Conduct site visits to assess performance and resolve issues
- Collaborate with cross-functional teams for accurate data collection and reporting
- Provide training and guidance to site staff and other CRAs
- Build and maintain relationships with site personnel and stakeholders
Zentrale Anforderungen
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate with strong knowledge of trial processes and regulations
- Ability to manage multiple sites and projects simultaneously with strong organizational skills
- Expertise in monitoring practices, data integrity, and site management; proficiency with clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills; ability to influence and drive compliance
- strong communication
- stakeholder management
- problem-solving
- monitoring practices
- data integrity
- site management
Clinical Research Associate 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.
