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    Clinical Data Manager - Philadelphia, United States - American College of Radiology

    American College of Radiology
    American College of Radiology Philadelphia, United States

    1 week ago

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    Full time
    Description

    Job Details

    Description

    The is a professional association serving over 42,000 members across the country. Consistent with the ACR's mission to advance the practice of radiology and improve the health outcomes of the populations we serve, the ACR's Center for Research and Innovation (CRI) has been a world leader in radiology clinical research for over 50 years. Over this period, the CRI has conducted clinical research trials and other research projects that have transformed the practice of radiology, informed the development of clinical practice standards, led to new device approvals, and changed healthcare policy.

    The CRI serves as the core radiology resource for NCI multicenter clinical trials involving diagnostic or therapeutic radiology. And, through active research committees in neuroradiology, cardiology, oncology, and pediatrics, the CRI has developed and delivered a diverse range of research studies in partnerships with academia and with commercial sponsors. Research studies range from prospective clinical trials to retrospective reader studies, clinical and imaging registries, novel imaging methods and imaging software, validation of biomarkers, radiomic feature analysis, and AI algorithm development and validation.

    Based on these strategic objectives, ACR is seeking a Clinical Data Manager to provide support to the ACR study initiatives across the College.

    Principal duties include:

  • Review protocols and coordinate study set-up activities for trials
  • Define data collection methods based on protocol aims
  • Collaborate with study team members and investigators to determine metadata specifications
  • Program forms within the EDC system as per specifications
  • Identify and program edit checks and web logic specifications
  • Create calendar specifications for data collection
  • Perform user acceptance testing
  • Prepare CRF and/or web entry completion guidelines
  • Create standard, study-specific, and ad hoc reports
  • Perform database updates as needed per protocol amendments
  • Perform quality control review checks to ensure data integrity
  • Serve as a resource for site research associates to ensure adherence to protocol specifications.

    • Qualified candidates will possess the following:

  • 3+ years of related experience preferred
  • Professional nursing degree/other healthcare certification/Bachelor's degree preferred
  • Experience in a multi-modality clinical trials group or research team a plus
  • Certified Medidata Rave Study Builder a plus.

    • If you would like to put your experience to great use in a professional team-oriented environment,

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