Clinical Research Associate II

Role: Clinical Research Associate (CRA) II responsible for monitoring clinical study activities to ensure compliance with GCP, SOPs, and study protocols. Objectives: oversee study site preparation, conduct in-clinic monitoring, and coordinate with CROs and vendors to meet project milestones. Responsibilities: supervise study start-up, site management, and documentation; act as liaison with vendors and cross-functional teams; contribute to protocol and study document development; participate in negotiations and study budgeting; evaluate CRO and site performance. Requirements: BS/BA in science or healthcare field or RN; 3+ years’ CRA experience, preferably in pharma or CRO environments; knowledge of clinical trials process, GCP, SOPs, and drug supply. Preferred skills include strong communication, multitasking, and technical proficiency with clinical trial tools. High-value: experience in oncology or hypercortisolism trials, GCP/regulatory compliance, site management, and vendor oversight. Work setup: onsite role based in the United States with no specified travel.