CRA II - Shanghai
Clinical Careers Page(19 hours ago)
About this role
A CRA II at Syneos Health is responsible for conducting monitoring activities for clinical trials, ensuring compliance with regulatory guidelines, maintaining accurate documentation, and supporting site and project management throughout the clinical study lifecycle. The role involves travel and collaboration with site personnel and project teams to facilitate successful trial execution.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Site Management
- Data Review
- Source Documentation
- Investigational Product
- Regulatory Compliance
- Communication
- Project Management
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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