Clinical Data Managers II

About the Role

This position is primarily a study lead Clinical Data Manager. It supports multiple clinical study teams by reviewing and/or completing study-related clinical data management deliverables. The role involves frequent interaction with study team members to troubleshoot, manage, and develop study-specific processes. The Clinical Data Manager actively participates in the development of processes and documents that support the clinical data management team.

Huntsman Cancer Institute is committed to cancer prevention, care, and survivorship for all communities within the area we serve—Idaho, Montana, Nevada, Utah, and Wyoming—with impact worldwide. Candidates are invited to share in their cover letter or interview how their professional experiences have prepared them to contribute to reducing the cancer burden experienced by all people and communities.

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-specific documents, including:
  • 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 timelines, deliverables, and/or data quality to the study team and functional supervisor.
• Manage and document the study-specific change control process and provide realistic feedback to the study team about the 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 of the project.
• Provide project-specific training on electronic data capture (EDC) and other data management systems to internal and external personnel.
• Discuss questions and suggestions for improvements with the study team prior to implementing new or modified study-specific processes.
• Assess current and proposed processes for compliance with regulations and standards, demonstrating a solid understanding of the regulatory framework as it relates to clinical research and data management.

This position is patient-sensitive and requires immunization according to CDC standards and hospital policy, with limited exemptions for documented medical contraindications or religious beliefs.

Work Environment

• Nearly Continuously: Office environment, sitting, hearing, listening, talking.
• Often: Repetitive hand motion (such as typing), walking.
• Seldom: Bending, reaching overhead.

Requirements

• Bachelor’s degree (or equivalency) + 4 years of directly related work experience or a master’s degree (or equivalency) + 2 years of directly related work experience.
• Understanding of basic regulations involving clinical trials, clinical data management, and clinical data systems.
• Ability to perform all data management activities associated with a clinical trial with a high degree of quality.
• Possess all skills, knowledge, and competencies required of the Clinical Data Manager I position.

Preferences

• Bachelor’s degree in life sciences, pharmacy, nursing, a related subject, or equivalency.
• Two or more years of relevant clinical data management experience.

Benefits

Learn more about the benefits of working for the University of Utah at benefits.utah.edu.

Pay

$54,807.25 per year.

Requisition Number: PRN45969B | Full-time | Open until 11/18/2026