Cardiac Data Processing Specialist

To support clinical trials, the Cardiac Data Processing Specialist will review and process cardiac data, ensuring quality and compliance with regulatory standards, while working either remotely or onsite in a full-time capacity. Key responsibilities Review and process cardiac data recordings according to study-specific protocols and data acquisition guides Perform data quality assurance and correction, ensuring accuracy and completeness of clinical trial data Communicate data discrepancies to trial sponsors and sites, resolving queries using the Query Management System Required qualifications Associate degree or higher in a relevant field (Life Sciences, Health Sciences, or related) 1-2 years of experience in data coordination, quality assurance, or clinical trials preferred Proficiency in Microsoft Office Suite and familiarity with clinical data systems Strong attention to detail and organizational skills Excellent communication and problem-solving abilities