Clinical Research Coordinator

Great benefits including health, dental, vision, 401k w/match and 15 days PTO Monday-Friday, On Site Schedule Seeking motivated candidates looking for a fast paced environment with growth opportunities! About Our Client Our client is a fast growing site network that currently has over 30 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: oncology, cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors. Responsibilities Coordinate all aspects of assigned clinical trials Perform study procedures such as phlebotomy, ECGs, and sample processing Conduct subject visits and ensure accurate, timely documentation in compliance with all applicable standards Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs Manage subject recruitment, informed consent, and retention activities Ensure timely EDC data entry and resolution of queries Report and follow up on AEs, SAEs, and protocol deviations Collaborate with investigators, sponsors/CROs, labs, and internal teams Prepare for and participate in monitoring visits, audits, and inspections Maintain regulatory documentation and ensure training compliance for amendments and systems Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory Qualifications: 2+ years of experience as a CRC with a research site #J-18808-Ljbffr