Clinical Research Associate II

📋 Description

• • The Clinical Research Associate II (CRA II) is a seasoned professional responsible for monitoring and site management in clinical research studies, ensuring patient safety, data quality, and protocol compliance across oncology or cardiology therapeutic areas.
• • Day-to-day responsibilities include conducting site visits (pre-study, initiation, routine, close-out), monitoring investigational product handling, reviewing source documents and EDC data, managing site start-up activities, verifying informed consent processes, identifying and reporting adverse events, maintaining trial master files, and communicating with site personnel and project teams to resolve protocol deviations and risks.
• • Precision for Medicine is a midsized, precision-focused CRO specializing in oncology and complex disease states, known for high CRA retention, strong work-life balance, reasonable travel, and a culture where employee voices are heard and valued through direct management support and professional growth opportunities.
• • In this role, you will deepen your expertise in clinical monitoring, GCP compliance, and therapeutic area knowledge while gaining influence in study execution, developing leadership in site management, and contributing to high-quality oncology and cardiology trials with opportunities for advancement and skill diversification.