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. It supports multiple clinical study teams 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. Huntsman Cancer Institute values cancer-related health equity and inclusion as integral to our guiding principle to serve our patients and their communities, and our commitment to foster a culture of belonging for all within our organization. This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job. This position is intended to be focused on study level activities with oversight from the manager of clinical data management. Employees are expected to be the independent representative of the clinical data management function on the cross functional study team.

Requirements

Bachelor’s degree in the life sciences, pharmacy, nursing, a related subject, or equivalency.
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.
Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description