CRA II - Beijing/Chengdu/Chongqing/Guangzhou
Clinical Careers Page(1 month ago)
About this role
CRA II at Syneos Health conducts clinical trial site activities across assigned regions in China, supporting study conduct from site qualification through close-out. The role focuses on ensuring regulatory and protocol compliance, protecting patient safety and data integrity, and collaborating with project teams and sponsors. It involves travel to investigator sites and participation in study meetings and training.
Required Skills
- Clinical Monitoring
- Site Management
- Site Initiation
- Regulatory Compliance
- ICH-GCP
- Source Review
- CRF Verification
- IP Management
- ISF Management
- Audit Readiness
+2 more
Qualifications
- Bachelor's Degree
- Registered Nurse (RN)
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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