(Senior) Clinical Research Associate - sponsor dedicated
On-site · Frankfurt am Main, Hesse, Germany
Job Summary
As a Senior Clinical Research Associate (CRA) at ICON Plc, you will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Key responsibilities include monitoring clinical trial sites, conducting site visits, collaborating with cross-functional teams, and providing training to site staff. Necessary qualifications include an advanced degree, extensive experience in clinical research, strong organizational skills, and fluency in both German and English. The role requires the ability to travel extensively and manage multiple sites effectively.
Required Qualifications
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements
- 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, interpersonal, and stakeholder management skills
- Fluency in German and English language
- Ability to travel at least 60% of the time
Additional Requirements
- All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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