CRA II
Clinical Careers Page(10 days ago)
About this role
A CRA II at Syneos Health performs site management activities for clinical trials, ensuring compliance with regulatory guidelines and maintaining communication with study sites. The role involves monitoring, data verification, and supporting study documentation to facilitate clinical research processes.
Required Skills
- GCP
- ICH Guidelines
- Regulatory Compliance
- Clinical Monitoring
- Data Verification
- Source Document Review
- Trial Management
- Investigator Site Files
- Pharmacovigilance
- Clinical Data
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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