Clinical Research Associate II (CRA II)| Germany| Hybrid
Core
Ensure successful delivery of clinical trials by managing site selection, initiation, monitoring, and close-out visits while maintaining GCP and regulatory compliance.
Role type
Senior IC clinical research associate (monitoring)
Builds
Clinical trials for healthcare/pharmaceutical clients
Domain
Life Sciences / Clinical Research
Deliverable
physical/clinical work
Required skills
Clinical trial monitoring, GCP/ICH-GCP compliance, site management, protocol deviation management, adverse event reporting, CRF review, regulatory approval tracking
Preferred skills
Onco-Haematology/Oncology trial experience, additional languages
Technologies
None stated
Responsibilities
Conduct site selection, initiation, monitoring, and close-out visits; Monitor study progress including patient recruitment and CRF completion; Review CRFs and manage query resolution; Ensure compliance with protocols and GCP guidelines; Report and follow up on adverse events; Manage protocol deviations and corrective action plans; Coordinate with investigative sites and external vendors; Support site payment management
Seniority
Mid-Senior, hands-on IC