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Posted 1mo ago•Essen
Clinical Research Associate II (CRA II)| Germany| Hybrid
JuniorOn-site (Essen)Salary undisclosed
Required Skills
Next.jsGCP
Job Description
Join us
As a Clinical Research Associate (CRA II), you will play a key role in ensuring the successful delivery of clinical trials while maintaining the highest standards of GCP, ICH-GCP compliance, and regulatory requirements. You will work closely with investigative sites, study teams and external partners to ensure studies are conducted efficiently, ethically and in accordance with protocol requirements.
Key Responsibilities
- Conduct and manage site selection, site initiation, monitoring and close-out visits.
- Ensure clinical trials are conducted in compliance with study protocols, Good Clinical Practice (GCP) guidelines, applicable regulations and standard operating procedures.
- Monitor study progress, including regulatory approvals, patient recruitment, CRF completion and query management.
- Review CRFs in line with the monitoring plan and study requirements.
- Support communication and coordination between investigative sites and external vendors, including central laboratories.
- Ensure appropriate reporting and follow-up of adverse events.
- Identify, document and suppor
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