Working remotely in a full-time capacity, the Research Data Coordinator III will manage protocol-specific data requirements for diverse and complex research projects, ensuring compliance with good clinical practices and federal regulations. Key responsibilities Review and synthesize information from medical records to extract data for industry, cooperative, and investigator-initiated trials Independently resolve data queries and provide support for high patient volume and trial complexity Collaborate with coordinators and study monitors to ensure accurate and timely data management Required qualifications High School Diploma/GED required; an Associate's degree with two years of research data management experience will be considered Four years of experience in research data management Experience with clinical trial management systems and electronic medical records (EMR) Preferred certification from SOCRA/ACRP or equivalent Expertise in data capture/reporting systems and medical record interpretation