A company is looking for a Clinical Data Coordinator for a remote, temporary position in Oncology research. Key Responsibilities Manage the abstraction, entry, and oversight of study data for clinical trials Assist with the collection, cleaning, and reporting of clinical research data Ensure compliance with protocol guidelines and maintain study-specific documentation Required Qualifications 3+ years of experience in data collection within a GCP / clinical research environment High School diploma required; some college preferred Experience in clinical studies, specifically in Oncology, for at least 6 months Familiarity with GCPs, ICH, and applicable federal regulations Experience with Medidata EDC systems and proficiency in Microsoft Office Suite
Clinical Coordinator • Carrollton, Texas, United States