Lead Clinical Data Manager for Cancer Trials

University of Utah; Salt Lake City (UT); On-site; USD 49,000 - 60,000; Full time

Job summary

University of Utah is seeking a Clinical Data Manager II to lead data management activities for multiple clinical studies. The role involves partnering with study teams to troubleshoot, develop study-specific processes, and manage essential CDM deliverables across the trial lifecycle.

The position emphasizes governing regulatory standards, cross-functional collaboration, and training others on EDC and related systems. Campus location with full‑time expectations.

Qualifications

• Bachelor's degree or higher in life sciences, pharmacy, nursing, or related field.
• Equivalent combination of education and experience may be considered.
• Experience with clinical data management and regulatory standards.

Responsibilities

• Participate in cross-functional project teams as the lead clinical data manager.
• Provide input in the design of protocols, forms, and data collection processes.
• Create and maintain study documents: Data Management Plans, Edit specifications, SAE Reconciliation Guidelines.
• Other plans and guidelines as required.
• Ensure documents are provided according to established timelines and SOPs.
• Communicate issues affecting timeline, deliverables, and data quality to the study team and supervisor.
• Manage study-specific change control process and provide feedback on impact of proposed changes.
• Review and provide feedback on other study-specific documents.
• Manage all data management activities of a clinical trial in the maintenance phase.
• Provide project-specific training on EDC and other data management systems to internal and external personnel.

Education

Bachelor's degree

Master's degree

Tools

EDC systems

Job description

University of Utah is seeking a Clinical Data Manager II to lead data management activities for multiple clinical studies. The role involves partnering with study teams to troubleshoot, develop study-specific processes, and manage essential CDM deliverables across the trial lifecycle.

The position emphasizes governing regulatory standards, cross-functional collaboration, and training others on EDC and related systems. Campus location with full‑time expectations.