Clinical Research Associate 1 - CFSP
Core
Conducting site selection, initiation, monitoring, and close-out visits for clinical trials while ensuring compliance with regulatory guidelines.
Role type
Junior Clinical Research Associate (monitoring)
Builds
Clinical trial data integrity and regulatory compliance for life sciences clients
Domain
Clinical research / Life sciences
Deliverable
client delivery
Required skills
Site monitoring, regulatory compliance (GCP/ICH), subject recruitment planning, data query resolution, regulatory submission tracking
Preferred skills
None stated
Technologies
MS Office
Responsibilities
Performing site selection, initiation, monitoring, and close-out visits; supporting subject recruitment plan development; evaluating site practices against GCP and ICH guidelines; tracking regulatory submissions, recruitment, and data queries; collaborating with study sites and client representatives
Seniority
Junior, entry-level IC