Clinical Research Associate (CRA) Germany
Core
Conduct on-site and remote clinical monitoring to ensure regulatory compliance, data integrity, and patient safety across drug development studies.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical sponsors
Domain
Life Sciences / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
ICH-GCP knowledge, site qualification, source document review, informed consent verification, investigational product management, audit readiness, data entry, travel management
Preferred skills
Real World Late Phase study experience, chart abstraction
Technologies
Electronic data capture systems, tracking systems
Responsibilities
Perform site qualification, initiation, interim monitoring, and close-out visits; verify informed consent and patient safety; conduct source document reviews and CRF data verification; manage investigational product inventory and administration; review Investigator Site Files; document activities and support recruitment; prepare for audits; attend investigator and sponsor meetings.
Seniority
Individual Contributor