Senior Clinical Research Associate

Role: Senior Clinical Research Associate (SCRA), focusing on site management and oversight in clinical trials. Responsibilities: monitor study sites to ensure data quality and patient safety per ICH-GCP; conduct visits, develop monitoring tools, track enrollment and study progress; support audits and inspections; mentor junior CRAs; collaborate with study teams to meet milestones and address quality issues. Requirements: BS/BA in a scientific field; 4-6 years of clinical operations experience, including 3-4 years monitoring in pharma or CRO; strong knowledge of ICH guidelines; excellent communication, organizational, and multitasking skills. Preferred: experience with global oncology trials. HighValue: oncology (cancer), clinical trial site management, GCP compliance, audit support, mentoring, travel up to 60%. WorkSetup: travel-intensive role (up to 60%).