Overview
As a Senior/CRA at ICON, you will oversee clinical trial activities to ensure protocol compliance, data integrity and participant safety. You will monitor sites, conduct visits, and collaborate with cross-functional teams to enable smooth trial execution. You’ll train and guide site staff, manage relationships with site personnel, and drive compliant, high-quality trial conduct. This role offers exposure to international sites and a fast-paced, impact‑driven environment that supports patient access to new medicines.
Leistungen / Benefits
- Competitive base salary
- Health and wellbeing programmes including medical, dental, and vision coverage
- 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
Verantwortungsbereiche
- Monitor trial sites for protocol adherence, regulatory compliance, and GCP
- 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 other CRAs
- Build and maintain relationships with site personnel and stakeholders to enable smooth operations
Zentrale Anforderungen
- Master's or Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills with attention to detail
- Ability to work independently and collaboratively in a fast-paced environment
- Experience managing multiple sites and projects simultaneously
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software/tools
- Excellent communication skills in German and English
- Excellent interpersonal and stakeholder management skills with ability to influence and drive compliance
- Ability to travel at least 60% of the time (international and domestic) and possess a valid driver’s license
- Legal right to work in the country of the role's location
- strong communication
- stakeholder management
- problem-solving
- monitoring practices
- data integrity
- site management
Clinical Research Associate II / Senior Clinical Research Associate Large Pharma/Biotech 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.
