CRA II - Sponsor Dedicated - Madrid/Barcelona, Spain
Clinical Careers Page(7 days ago)
About this role
A CRA II at Syneos Health supports clinical trial activities across various phases, ensuring compliance with regulatory standards, maintaining documentation, and liaising with site personnel. The role involves on-site and remote monitoring, data review, and site management, contributing to the successful execution of clinical studies in the biopharmaceutical field.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Site Management
- Data Review
- Regulatory Compliance
- Source Document Review
- Investigator Site Files
- Pharmacovigilance
- Clinical Trials
About Clinical Careers Page
syneoshealth.comSyneos Health is a biopharma solutions organization and full‑service contract research organization (CRO) that integrates clinical development, regulatory and commercialization services to help life‑science companies bring therapies to market faster. It provides end‑to‑end capabilities — clinical trials across phases and therapeutic areas, real‑world evidence and data analytics, medical affairs, market access, patient engagement and commercial launch services. With a global network of scientific, clinical and commercial experts, Syneos partners with biopharma, biotech and medtech clients to de‑risk development programs and accelerate product adoption.
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