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Job type full-time
Benefits pulled from the full job description
403(b) paid time off tuition reimbursement
Not provided by employer
Full job description
The american college of radiology is a professional association serving over 40,000 members across the countryConsistent 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 yearsOver this period, the cri has conducted clinical research trials and other research projects which 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 radiologyAnd, 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 sponsorsResearch 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 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 online 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 preferredProfessional 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, please apply onlineTo learn more about acr’s rewarding employee experience, culture, and benefits, visit: https://www.acr.org/about-acr/work-with-us
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.
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Job type: full-time
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Posted 4 days ago
