Clinical Research Associate III

Position Overview: Site Monitoring & Management Independently manage 10–15 investigational sites from start-up through close-out Perform all monitoring visits (SIV, IMV, COV) in accordance with the Monitoring Plan Ensure compliance with protocol, Monitoring Plan, SOPs, and applicable regulations (ISO 14155, FDA, and local requirements) Conduct SDV/SDR, informed consent review, and AE/SAE oversight Maintain full ownership of assigned investigator sites, ensuring successful site management and performance Build and maintain strong relationships with Principal Investigators and site staff Provide training, guidance, and ongoing support to site personnel Communicate effectively to manage queries, provide updates, and drive issue resolution Ensure data quality, timely query resolution, and site compliance Identify risks and support audit and inspection readiness Collaborate cross-functionally with Data Management, Clinical, and Project Management teams to support study execution Attend Investigator and/or Coordinator meetings Team Support & Mentorship Share expertise and provide guidance to junior CRAs, serving as a resource for questions, problem-solving, and best practices Support training initiatives and review work, contributing to team development and consistency across sites Provide support to upper management as needed, including contributing to study updates, escalations, and operational decision-making Qualifications: 5+ years of CRA experience Strong medical device experience Medical device experience, cardiovascular/TEVAR preferred Solid understanding of GCP and FDA regulatory requirements Ability to work independently and effectively multitask, prioritizing competing activities across multiple sites and study demands 50-75% of travel is required for this position. #J-18808-Ljbffr Regulatory Jobs