Clinical Research Associate 2 - Multi-Sponsor - Based in Madrid or Barcelona
Core
Conducting site selection, initiation, monitoring, and close-out visits for clinical trials while ensuring data integrity and regulatory compliance.
Role type
Junior Clinical Research Associate
Builds
Clinical trial data and patient recruitment plans
Domain
Life sciences / Clinical research
Deliverable
client delivery
Required skills
Site monitoring, regulatory compliance (GCP/ICH), subject recruitment planning, data query resolution, travel management
Preferred skills
MS Office proficiency, problem-solving, time management
Technologies
MS Office
Responsibilities
Perform site selection, initiation, monitoring and close-out visits; Support subject recruitment plan development; Evaluate site practices against GCP/ICH guidelines; Track regulatory submissions, recruitment, and data queries; Collaborate with study sites and client representatives
Seniority
Junior, hands-on IC
