Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)
Core
Monitor clinical trial sites to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability and subject safety.
Role type
Junior Clinical Research Associate (CRA I)
Builds
End-to-end clinical trial programs for commercial and government clients
Domain
Life Sciences / Clinical Research / Regulatory Compliance
Deliverable
client delivery
Required skills
Clinical monitoring, ICH-GCP guidelines, risk-based monitoring, root cause analysis, data accuracy verification, site initiation, trial close-out, regulatory compliance
Preferred skills
Medical/therapeutic area knowledge, Microsoft Office proficiency, process improvement
Technologies
Clinical Trial Management System (CTMS)
Responsibilities
Conduct on-site and remote monitoring visits, assess protocol and regulatory compliance, manage investigator site relationships, ensure audit readiness, track trial status and progress, participate in investigator meetings, handle investigator payment processes, maintain essential study documents, perform QC checks on system reports.
Seniority
Junior, hands-on IC