Clinical Research Associate I (CRA)
Core
Conduct onsite and remote monitoring visits, review case report forms, verify source documents, and resolve queries to ensure data integrity and compliance with study protocols.
Role type
Junior Clinical Research Associate (CRA)
Builds
Clinical trial data and regulatory compliance for pharmaceutical sponsors
Domain
Clinical research / Pharmaceutical industry
Required skills
Good Clinical Practice (GCP) knowledge, clinical trial process understanding, site communication, documentation management, query resolution, source document verification
Preferred skills
Prior clinical research experience, advanced CRA/Clinical Monitoring training
Technologies
mibeg, Pharmaakademie
Responsibilities
Conduct onsite and remote monitoring visits, perform CRF review and source document verification, maintain trial documentation, manage site communication, assist in site identification
Seniority
Junior, entry-level IC