Clinical Data Management Associate II
Core
Review, validate, and manage clinical trial data generated from imaging studies to ensure quality, accuracy, and integrity for life-changing therapies.
Role type
Mid-level IC clinical data management associate (medical imaging)
Builds
Reliable clinical data and audit-ready study documentation for medical imaging studies
Domain
Healthcare + Clinical Research (Medical Imaging)
Required skills
Clinical trial processes, data review methodologies, clinical database management, relational database concepts, data validation techniques, quality control processes, data specifications, edit checks, data transfer requirements, study configuration documentation, clinical trial terminology, Microsoft Office (Word, Excel, Access, Outlook, PowerPoint), analytical problem-solving, attention to detail, organizational skills, time management, written communication in English
Preferred skills
Experience developing/maintaining data specifications, edit checks, data transfer requirements, or study configuration documentation, familiarity with regulated research environments
Technologies
Microsoft Office (Word, Excel, Access, Outlook, PowerPoint)
Responsibilities
Review study documentation and assess impacts on data management processes, support study setup and data collection strategies, implement and execute data management plans, define and maintain edit checks, review clinical and imaging data for inconsistencies, develop and maintain study data specifications, create and maintain transmittal forms and study documentation, investigate and resolve data discrepancies, track data-related issues to resolution, prepare and validate ad hoc data listings and reports, identify system enhancements or process improvements, maintain audit-ready study documentation, communicate project status and risks, contribute to SOP updates and quality initiatives, support compliance with GCP and regulatory expectations
Seniority
Mid-level, hands-on IC
