Experienced CRA (m/w/d), Multi Sponsor, home-based Austria
Core
Conduct monitoring on complex clinical trials for different pharma companies, ensuring adherence to GCP and study protocols while managing site relationships and trial progress.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial operations for diverse pharma sponsors
Domain
Life sciences / Clinical research
Required skills
Site selection and initiation, monitoring visits, subject recruitment planning, regulatory compliance (GCP/ICH), data query resolution, stakeholder collaboration
Preferred skills
Experience as CRA, Study Coordinator, or Nurse
Technologies
GCP, ICH guidelines, CRF systems
Responsibilities
Perform site selection, initiation, monitoring, and close-out visits; Support subject recruitment plan development; Evaluate site practices for regulatory compliance; Manage trial progress tracking (submissions, recruitment, CRF, data queries); Collaborate with study sites and client representatives
Seniority
Mid-to-Senior, hands-on IC
