We are seeking an experienced Clinical Research Associate II (CRA II) based in Brazil to support and oversee clinical trial activities across oncology studies and additional therapeutic areas. The ideal candidate will bring 10+ years of CRA experience , including strong exposure to all phases of clinical trials (Phase I–IV) within a CRO environment .

This role requires a highly motivated professional with excellent site management capabilities, deep understanding of ICH‑GCP guidelines, and strong communication skills in both English and Spanish.

Key Responsibilities

• Conduct and oversee all clinical monitoring activities across Phase I–IV oncology and multi‑therapeutic clinical trials in compliance with ICH‑GCP, ANVISA regulations, protocol requirements, and sponsor SOPs.
• Independently manage investigative sites from start‑up through close‑out, ensuring data integrity, patient safety, and regulatory compliance...