Clinical Research Associate 2 , Multi-Sponsor - Based in Portugal
Core
Conducting site selection, initiation, monitoring, and close-out visits for clinical trials while ensuring compliance with Good Clinical Practice and ICH guidelines.
Role type
Clinical Research Associate (monitoring)
Builds
Clinical trial data and regulatory submissions for life sciences clients
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Site monitoring, subject recruitment planning, regulatory compliance, data query resolution, travel management
Preferred skills
MS Office proficiency, organizational skills, problem-solving
Technologies
MS Office
Responsibilities
Performing site selection, initiation, monitoring, and close-out visits; Supporting subject recruitment plan development; Evaluating site practices for regulatory compliance; Managing progress on regulatory submissions, recruitment, and data queries
Seniority
Mid-level, hands-on IC
