Clinical Research Associate - Sponsor Dedicated

Role: Clinical Research Associate specializing in sponsor-dedicated site monitoring and management for clinical trials. Responsibilities: Conduct site visits (initiation, ongoing, closeout), develop and monitor recruitment plans, provide protocol training, ensure site compliance with protocols and regulations, and track study progress including regulatory submissions, enrollment, CRF completion, and data queries. Qualifications & Skills: Bachelor's degree in scientific or healthcare field preferred, with at least 1.5 years of on-site clinical trial monitoring experience. Knowledge of Good Clinical Practice and ICH guidelines is essential. Proficiency in Microsoft Office and strong communication skills in English are required. Organizational and problem-solving abilities, along with the capacity to build effective stakeholder relationships, are important for success. Compensation: $90,200–$190,000 base.