CRA single sponsor - Germany
Clinical Careers Page(4 days ago)
About this role
This role involves overseeing clinical site activities such as qualification, initiation, monitoring, and close-out to ensure compliance with regulations and protocols. The position supports data accuracy, patient safety, and study progress while collaborating with site personnel and project teams. It may also include responsibilities related to real-world late phase studies.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Site Management
- Source Documentation
- Data Reconciliation
- Investigator Site File
- Protocol Compliance
- IP Inventory
- Regulatory Knowledge
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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