Elevate your career as a Clinical Research Associate specializing in Oncology with Prevail. This remote role focuses on monitoring Phase I-IV studies and requires expertise in Breast Cancer research.
Join Prevail, where you'll independently manage site activities and ensure compliance with protocols and regulations for clinical research. Your expertise in ICH-GCP and experience in site management will be vital as you evaluate site performance and escalate issues timely. This role provides a unique opportunity to integrate your knowledge with practical site-level operations in breast cancer studies.
Key Responsibilities:
• Initiate and manage sites for clinical trials
• Evaluate site performance and staff efficiency
• Ensure regulatory compliance and protocol adherence
• Document activities through communication logs and reports
• Support subject recruitment and retention strategies
Requirements:
• Experience as a Clinical Research Associate
• Knowledge of ...