Single Sponsor CRA I / II (Must have UK monitoring exp. Phase I exp. preferred.)
Clinical Careers Page(13 days ago)
About this role
A Single Sponsor CRA I / II is responsible for site monitoring and management activities during clinical trials, ensuring compliance with regulatory standards such as ICH-GCP. The role involves remote and on-site visits, data verification, site support, and collaboration with various project stakeholders to help facilitate successful clinical study execution.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Data Review
- Site Management
- Regulatory Compliance
- IP Inventory
- Source Document Review
- Trial Management
- Remote Monitoring
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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