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Clinical Research Associate III

Artivion • Kennesaw, GA, US • published 2026-10-29 21:15:52.583754

Description

**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, prob...

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