About this role
Freelance CRA - Spain at Iqvia. Location: Madrid or Barcelona. Role: monitoring trials, conducting visits, reviewing data Requirements: Experience monitoring clinical trials, site initiation/evaluation/close-out visits, GCP/ICH knowledge, eCRF/EDC use, strong communication and independent judgment. Category: Research and Development (R&D) Seniority: Mid Level Tools: eCRF, EDC Commitment: Part Time Workplace: Field Languages: English