CRA I/CRA II (m/f/d) - FSP Germany
Core
Managing clinical trial sites across Germany to ensure compliance with protocols, ICH-GCP, and regulations.
Role type
Clinical Research Associate (CRA)
Builds
High-quality, inspection-ready clinical trials
Domain
Clinical research / Life sciences
Deliverable
client delivery
Required skills
Independent site monitoring, risk-based monitoring, protocol compliance, ICH-GCP knowledge, regulatory compliance, CRF review, investigational product accountability, root cause analysis, CAPA principles, audit readiness, data quality management, study system management (CTMS), investigator identification, site initiation, study close-out
Preferred skills
Process improvement, mentoring
Technologies
CTMS
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