Clinical Research Associate (CRA)
Core
Conduct clinical trials by performing site visits, monitoring compliance, and managing study documentation to ensure data integrity and regulatory adherence.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data and regulatory compliance for pharmaceutical and biotechnology clients
Domain
Clinical research / Biomedical
Deliverable
client delivery
Required skills
GCP knowledge, clinical trial regulations, site monitoring, patient recruitment oversight, query management, adverse event reporting, protocol deviation management
Preferred skills
Italian language, additional languages
Technologies
Clinical trial management systems (implied via CRF/query management)
Responsibilities
Perform site selection, initiation, monitoring, and close-out visits; oversee patient recruitment and CRF completion; manage communication with external vendors; ensure accurate adverse event reporting; maintain study documentation and files
Seniority
Individual Contributor