Research Data Coordinator III

Working remotely in a full-time capacity, the Research Data Coordinator III will manage protocol-specific data requirements for complex research projects, ensuring compliance with good clinical practices and federal regulations while synthesizing information from various medical records. Key responsibilities Extract and synthesize data from medical records, including clinic notes and pathology reports, as per assigned research protocols Independently resolve data queries and provide support for higher patient volume and trial complexity Collaborate with coordinators and monitors, ensuring data integrity and compliance with regulatory standards Required qualifications High School Diploma/GED with four years of research data management experience, or an associate degree with two years of relevant experience Experience with clinical trial management systems and electronic medical records (EMR) Ability to interpret medical records and maintain confidentiality of subject data Demonstrated competency in data management and reporting systems Effective verbal and written communication skills, with the ability to train other data coordinators