Research Data Coordinator

Job Summary

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 is committed
to cancer prevention, care, and survivorship for all communities within the area we serve – which includes Idaho, Montana, Nevada, Utah, and
Wyoming – with impact worldwide.

In your cover letter or during your interview process, we invite you to share how your
professional experiences have prepared you to serve as a member of our team as we work to reduce the cancer burden experienced by all people
and communities. This may include description of your prior experiences related to research, prevention, clinical care, community
engagement/outreach, training, administration, or other areas relevant to Huntsman Cancer Institute’s mission and this position.

Responsibilities

1. Participate in the cross-functional project teams as the lead clinical data manager.
2. Provide input in the design of protocols, forms, and data collection processes.
3. Create and maintain the following study
   specific documents:
   1. Data Management Plans
   2. Edit specifications
   3. SAE Reconciliation
      Guidelines
   
   
4. Other plans and guidelines as required
5. Ensure documents are provided according to established
   timelines and SOPs.
6. Communicate issues that affect timeline, deliverables, and/or data quality to the study team and functional
   supervisor.
7. Manage and document the study specific change control process and provide realistic feedback to the study team about
   impact of proposed changes.
8. Review and provide feedback on other study specific documents.
9. Manage all data management
   activities of a clinical trial in the maintenance phase of the project.
10. Provide project specific training on electronic data
    capture (EDC) and other data management systems to internal and external personnel.

Problem SolvingEmployees in
this position are required to discuss questions and suggestion for improvements with the study team prior to implementing new or modified
study specific processes. The Clinical Data Manager II is expected to have a solid understanding of the regulatory framework as it relates
to clinical research and data management, and be able to assess current and proposed processes for compliance with regulations and
standards.

CommentsThis 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.

Work Environment and Level of Frequency typically requiredNearly Continuously: Office
environment.
Physical Requirements and Level of Frequency that may be required Nearly Continuously: Sitting, hearing,
listening, talking.Often: Repetitive hand motion (such as typing), walking.Seldom: Bending, reaching overhead.

Minimum
Qualifications
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.

Preferences

Special Instructions

Requisition Number: PRN44215B
Full Time or
Part Time? Full Time
Work Schedule Summary:
Department: 01167 – HCI Clinical Trials Operations
Location:
Campus
Pay Rate Range: 39300 to 72700
Close Date: 6/3/2026
Open Until Filled:

To apply, visit https://utah.peopleadmin.com/postings/196191

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