Clinical Data Manager

Job not on LinkedIn

🔥 0 minutes ago

🔔 Pennsylvania – Remote

🔔 Pennsylvania – Remote

💵 $73k - $80k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

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American College of Radiology

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 1924

🏥 Healthcare

💼 Consulting

🤝 Non-profit

Healthcare • Consulting • Non-profit

American College of Radiology is a professional medical society and nonprofit organization that supports radiologists and medical imaging professionals through education, accreditation, clinical guidance, research, data registries, informatics and advocacy. It provides continuing medical education and training, publishes the Journal of the American College of Radiology, manages accreditation programs and reporting/data systems for imaging facilities, develops AI and data-science resources for imaging, and represents radiology interests in policy and reimbursement discussions to improve patient care and imaging quality.

📋 Description

• Review study protocols and lead clinical data management activities during study startup • Design data collection strategies aligned with protocol objectives and study endpoints • Collaborate with investigators and research teams to develop metadata and data capture specifications • Partner with Clinical Data Programming staff to configure and validate electronic data capture (EDC) systems • Develop edit checks, web logic, and validation specifications to promote data quality and consistency • Create study calendars and data collection schedules • Conduct Operational Qualification (OQ) and Performance Qualification (PQ) testing of databases and study systems • Develop case report form (CRF) completion guidelines and user documentation • Produce standard, study-specific, and ad hoc reports to support study oversight and decision-making • Define and document database modifications required to support protocol amendments and study changes • Perform quality control reviews to ensure data accuracy, completeness, and regulatory compliance • Serve as a resource for site research staff, providing guidance on protocol requirements and data collection procedures

🎯 Requirements

• 3+ years of related experience preferred • Professional nursing degree, other healthcare certification, or bachelor's degree preferred • Experience in a multi-modality clinical trials group or research team a plus • Knowledge of CDASH/CDISC Standards a plus • Experience with electronic data capture (EDC) platforms required • Certified Medidata Rave Study Builder a plus • Strong attention to detail and commitment to data quality and process excellence required • Excellent organizational, communication, and collaboration skills required • Ability to manage multiple priorities in a fast-paced, team-oriented environment required

🏖️ Benefits

• Defined contribution pension plan • 403(b) • Generous paid time off package • Insurance plans with leading providers • Flexible spending • Tuition reimbursement • Training opportunities • Wellness reimbursement • Professional growth potential • Competitive compensation • Exceptional benefits package