PS Clinical Data Manager II

The University of Utah • Salt Lake, UT

14d

About The Position

This position is primarily a study lead Clinical Data Manager. The position will be assigned to the Salt Lake City VA project entitled, “Reducing Chronic Opioid Use Among veterans Undergoing Community Care Surgery Using a Transitional Pain Service”. The position will be assigned to the Salt Lake City VA. The position supports the study team by reviewing and/or completing study related clinical data management deliverables. Frequently interacts with study team members to troubleshoot, manage, and develop study specific processes. Actively participates in the development of processes, and documents, that support the clinical data management team. This individual will be an experienced data manager. They will ensure consistent and accurate data availability to end-users, control privileges and permissions, and monitor database performance. They will be responsible to devise methods and procedures for preparing data for statistical analysis and to conduct analysis as required. Additionally, all database security will be maintained by this individual including familiarity with VA data security and privacy policies and adherence to these regulations in manipulating, preparing, disseminating, and analyzing study data.

Requirements

• Bachelor’s degree in the life sciences, pharmacy, nursing, a related subject, or equivalency (one year of education can be substituted for two years of related work experience).
• Requires two or more years of relevant clinical data management 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 CDM I position.
• This position is patient-sensitive and must fulfill all associated requirements.
• We protect our patients, coworkers and community by requiring all patient-sensitive employees to be immunized according to CDC standards and hospital policy. Limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations.

Responsibilities

• Participate in the 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 the following study specific 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 that affect timeline, 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 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees