CRA II
Clinical Careers Page(11 days ago)
About this role
The CRA II at Syneos Health is responsible for site monitoring, management activities, and ensuring compliance with regulatory and protocol standards within clinical research. They support the full lifecycle of clinical trials, from site initiation to close-out, often working remotely or on-site, with an emphasis on data integrity and patient safety.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Regulatory Compliance
- Data Management
- Site Management
- Communication
- Investigator Relations
- Trial Coordination
- Pharmacovigilance
Qualifications
- Bachelor’s degree or RN in a related field
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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