Clinical Research Associate II / Senior Clinical Research Associate Large Pharma
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 compliance with protocols, regulatory requirements, and industry standards. Responsibilities include monitoring clinical trial sites for adherence to Good Clinical Practice (GCP), conducting site visits, collaborating with cross-functional teams for data collection, and providing training to site staff. You will maintain relationships with site personnel to facilitate trial operations. To qualify, you must have a Master or Bachelor's degree in a related field, at least 2 years of CRA experience, and strong communication skills in both German and English.
Required Qualifications
- Master or Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- Excellent communication skills in German and English
- Ability to travel at least 60% of the time
- Proven ability to manage multiple sites and projects simultaneously
Desired Qualifications
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Proficiency in relevant clinical trial software and tools
- Strong organizational skills
- Strong problem-solving skills
Additional Requirements
- Ability to influence and drive compliance within a complex environment
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