CRA I with at least 1 year of monitoring experience - Sponsor dedicated - Brazil remote

Clinical Careers Page(19 hours ago)

RemoteFull TimeJunior$60,000 - $70,000Clinical Operations

About this role

A CRA I at Syneos Health supports clinical trial monitoring activities, ensuring compliance with regulatory standards such as ICH-GCP and GPP. The role involves site management, data verification, and collaborating with site staff throughout the clinical trial process, including real-world late phase studies. The position offers opportunities for career development within a global biopharmaceutical solutions organization.

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Required Skills

GCP
ICH Guidelines
Clinical Monitoring
Data Verification
Site Management
Regulatory Compliance
CRA
Clinical Trials
Microsoft Office
Data Collection

About Clinical Careers Page

syneoshealth.com

Syneos 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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