Clinical Research Associate II

📋 Description

• • The Clinical Research Associate II (CRA II) role at Precision Medicine Group supports clinical trial execution by ensuring patient safety, data quality, and regulatory compliance across oncology and rare disease studies. This position is critical to advancing life-changing therapies by integrating clinical operations with scientific rigor and data science expertise.
• • Day-to-day responsibilities include conducting site visits (initiation, routine monitoring, close-out), verifying informed consent processes, reviewing case report forms, managing investigational product accountability, identifying and reporting serious adverse events, maintaining trial master files, and communicating with study sites and internal teams to resolve protocol deviations and risks.
• • Precision Medicine Group is a specialized CRO focused on oncology and rare disease, combining clinical trial execution with laboratory expertise, advanced data sciences, and operational scale to improve therapy development speed, cost, and success rates. The company emphasizes quality, compliance, and innovation in global clinical research.
• • The CRA II will develop advanced clinical monitoring skills, deepen expertise in oncology and rare disease trials, gain experience in global trial management, and strengthen abilities in risk-based monitoring, regulatory documentation, and cross-functional collaboration — preparing for senior clinical research roles.