FSO CRA II / Sr CRA
Clinical Careers Page(17 days ago)
About this role
Syneos Health is seeking a CRA to perform site management and monitoring activities for clinical trials, ensuring regulatory compliance and data integrity. The role involves collaborating with sites, managing documentation, and supporting study lifecycle activities.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Source Document Review
- Data Management
- Regulatory Compliance
- IP Management
- TMF
- Site Management
- Pharmacovigilance
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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