Sr CRA - Beijing/Shanghai/Guangzhou/Chengdu
Clinical Careers Page(19 days ago)
About this role
A Senior Clinical Research Associate (Sr CRA) at Syneos Health is responsible for monitoring clinical trial sites to ensure compliance with regulatory standards, protocols, and quality data collection. The role involves managing site activities, supporting regulatory compliance, and collaborating with cross-functional teams to facilitate clinical study progress across various locations in China.
Required Skills
- GCP
- ICH Guidelines
- Regulatory Compliance
- Clinical Monitoring
- Investigator Site Management
- Source Document Review
- Data Reconciliation
- IP Inventory
- CRF Data Entry
- Trial 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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