CRA I - Sponsor dedicated - Home Based Paris Area
Clinical Careers Page(5 days ago)
About this role
The CRA I role at Syneos Health involves performing clinical site management activities such as site qualification, initiation, monitoring, and close-out, either remotely or on-site, ensuring compliance with regulatory standards and company SOPs. The position supports clinical trial progress, data integrity, and site personnel training, contributing to the successful conduct of pharmaceutical studies.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Data Management
- Regulatory Compliance
- Source Document Review
- Investigator Site File
- Pharmacovigilance
- Trial Management
- Communication
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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