CRA II
Clinical Careers Page(4 days ago)
About this role
The CRA II at Syneos Health is responsible for site management activities in clinical trials, ensuring protocol compliance and data integrity. The role involves monitoring, site qualification, documentation review, and supporting study lifecycle activities with a focus on regulatory adherence and site coordination.
Required Skills
- GCP
- Clinical Monitoring
- Regulatory Compliance
- Source Document Review
- Data Management
- Investigator Site Files
- Informed Consent
- Pharmacovigilance
- Trial Management
- Site 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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