Clinical Research Coordinator-260129

We are seeking a detail-oriented and collaborative Clinical Research Coordinator in San Antonio, TX. You will drive study operations, maintain protocol compliance, and manage active trial execution across a dynamic clinical caseload. Responsibilities Coordinate all aspects of participant care from screening through study completion, including administering detailed informed consent and providing protocol-based subject education on investigational product (IP) use and safety. Dispense and administer investigational product (IP) while promptly tracking and reporting adverse events, protocol deviations, and safety issues to the PI, Sponsor, and IRB. Perform accurate and timely data collection, source documentation, and entry into databases, sponsor CRFs, and IWRS, while maintaining Essential Documents. Collaborate closely with the clinical team and external industry partners to ensure efficient trial selection, patient recruitment, and achievement of target enrollment goals. Assist in the preparation and facilitation of site initiation meetings, monitoring visits, and regulatory authority inspections. Manage the patient stipend automated payment process and ensure strict adherence to HIPAA, FDA GCP, and internal quality assurance guidelines. Required Skills 3+ years of clinical research experience as a CRC supporting investigational drug studies. Previous experience in a patient-facing research role, or experience as a Medical Assistant, EMT, or Phlebotomist. Proven ability to successfully support and manage at least 3 active studies simultaneously (industry-funded and IIT). #J-18808-Ljbffr Medix™