Research Data Coordinator II

Working remotely in a full-time capacity, the Research Data Coordinator II will autonomously review and synthesize medical records to extract trial data for multiple research projects, ensuring compliance with federal regulations and good clinical practices. Key responsibilities Review and synthesize information from medical records to extract data as per research protocols Determine methods and procedures related to data requirements and query resolution Collaborate with study coordinators and monitors to ensure alignment with protocol requirements Required qualifications High School Diploma/GED with three years of data management experience, or an AA/AS degree plus one year of clinical or research data management Experience in using automated data processing techniques and database software programs Ability to interpret all components of medical records and maintain confidentiality of subject data Effective verbal and written communication skills, with the ability to interact with healthcare professionals Experience in an oncology research setting is preferred Experience: 3 years required