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Clinical Research Coordinator

Central Texas Clinical Research • Austin, TX, US • published 2026-09-30 01:58:36.371290

Description

The **Clinical Research Study Coordinator (CRC)** manages the daily operational, administrative, and clinical logistics of multiple simultaneous complex clinical trials at our high\-volume research site. Working directly under the Principal Investigator (PI), you will serve as the central hub connecting patients, sponsors, Contract Research Organizations (CROs), and medical staff. This role requires an agile professional capable of maintaining rigorous Good Clinical Practice (GCP) compliance, maximizing patient retention, and managing flawless high\-density data entry in a fast\-paced environment. **Responsibilities**: **Patient Management \& Clinical Execution** * **Patient Recruitment:** Screen large\-scale electronic health records (EHR) and databases to identify, target, and recruit qualified study candidates. * **Informed Consent:** Guide candidates through the complex informed consent process, detailing study protocols, risks, and benefits in accessible language. * **Visit Coordination:** Schedule and orchestrate high\-frequency patient study visits, aligning procedures with strict protocol\-mandated timelines. * **Clinical Procedures:** Perform basic clinical tasks including...

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