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/ICH-GCP compliance.
Role type
Senior IC clinical research associate (monitoring) (via careerplan.io/jobs/2725358-clinical-research-associate-ii-cra-ii-germany-hybrid)
Builds
Clinical trials for healthcare/pharmaceutical clients
Domain
Life sciences / Clinical research
Deliverable
physical/clinical work
Required skills
GCP/ICH-GCP knowledge, site monitoring, protocol deviation management, adverse event reporting, CRF review, regulatory compliance
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 in line with monitoring plans; Ensure appropriate reporting and follow-up of adverse events; Identify and document protocol deviations; Support site payment management activities
Seniority
Mid-Senior, hands-on IC