CRA single sponsor - Germany
Clinical Careers Page(7 days ago)
About this role
A Clinical Research Associate (CRA) at Syneos Health supports clinical trial sites by performing monitoring activities, ensuring compliance with regulatory standards, and managing site-related documentation and processes. The role involves close collaboration with clinical sites and internal teams to facilitate efficient trial execution within regulatory guidelines.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Regulatory Compliance
- Data Management
- GMP
- Investigator Site Management
- Clinical Trials
- Medical Records
- Pharmacovigilance
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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