Sr CRA (Multi-sponsor) - Brazil Home Based
Clinical Careers Page(19 days ago)
About this role
A Senior Clinical Research Associate at Syneos Health conducts and supervises site activities for clinical trials, ensuring compliance with regulatory standards and protocol requirements. The role involves coordinating with site personnel, monitoring study progress, and supporting audit readiness, with a focus on real-world late phase studies.
Required Skills
- GCP
- ICH Guidelines
- Regulatory Requirements
- Clinical Monitoring
- Source Document Review
- Data Management
- Informed Consent
- Pharmacovigilance
- Trial Management
- Clinical Operations
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.
View more jobs at Clinical Careers Page →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Clinical Careers Page
Associate Project Director (Queensland based)
Clinical Careers Page(1 day ago)
Director, Safety & PV (Veeva Safety Implementation & Operations)
Clinical Careers Page(4 days ago)
Sponsor Dedicated Clinical Trial Manager - Home based EMEA, Hebrew Speaker
Clinical Careers Page(4 days ago)
Sr CRA - Sponsor-dedicated (Poland)
Clinical Careers Page(4 days ago)