Clinical Data Manager (Remote)

The American College of Radiology is a professional association serving over 42,000 members nationwide.  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 is 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 commercial sponsors.  Research studies range from prospective clinical trials to retrospective reader studies, novel imaging methods and imaging software, validation of biomarkers, radiomic feature analysis, and AI algorithm development and validation.

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

As a member of the ACR team you will:

• 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
• Collaborate with the Clinical Data Programming Team to program forms within the EDC system as per specifications
• Create edit check and web logic specifications
• Create calendar specifications for data collection
• Perform Operational and Performance Qualification testing
• Prepare CRF and/or web data entry completion guidelines
• Create standard, study-specific, and ad hoc reports
• Create specifications for database updates as needed to meet protocol amendment requirements

• 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
• Knowledge of CDASH/CDISC Standards 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, please apply online. To learn more about ACR’s rewarding employee experience, culture, and benefits, visit: https://www.acr.org/About-ACR/Work-With-Us

ACR is committed to a total rewards compensation philosophy that includes base salary in addition to our full suite of comprehensive benefits.  ACR’s goal is to pay competitively and equitably.  It is typical for individuals to be hired in the entry to middle of the range for their role, and compensation decisions depend on each case’s circumstances.  A reasonable estimate of the annual compensation range for this position is 71-95k.  

ACR offers a rewarding employee experience: innovative culture, professional growth potential, competitive compensation, and an exceptional benefits package, including a defined contribution pension plan, 403(b); generous paid time off package; insurance plans with the leading providers; flexible spending; tuition reimbursement; training opportunities; and wellness reimbursement.