University of Utah
Overview
Join to apply for the
PS Resrch Data Coordinator
role at
University of Utah .
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, with impact worldwide. We invite you to share how your experiences have prepared you to serve as a member of our team in reducing the cancer burden, including 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
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.
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.
Work Environment and Physical Requirements Work Environment : Nearly Continuously in office setting.
Physical Requirements : Nearly Continuously: Sitting, hearing, listening, talking. Often: Repetitive hand motion (such as typing), walking. Seldom: Bending, reaching overhead.
Additional Details Requisition Number:
PRN43957B
Full Time or Part Time?
Full Time
Department:
01167 - HCI Clinical Trials Operations
Location:
Campus
Pay Rate Range:
39300 to 72700
Close Date:
3/31/2026
How to apply To apply, visit
https://utah.peopleadmin.com/postings/194554
Open to qualified applicants. This description is intended to describe the general nature and level of work and is not a comprehensive list of duties and responsibilities.
Posted by the FREE value-added recruitment advertising agency.
Job Function
Information Technology
Industries
Higher Education
Note: This refined description preserves the core content while removing boilerplate, reorganizing into clear sections, and ensuring proper HTML structure with allowed tags.
#J-18808-Ljbffr
PS Resrch Data Coordinator
role at
University of Utah .
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, with impact worldwide. We invite you to share how your experiences have prepared you to serve as a member of our team in reducing the cancer burden, including 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
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.
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.
Work Environment and Physical Requirements Work Environment : Nearly Continuously in office setting.
Physical Requirements : Nearly Continuously: Sitting, hearing, listening, talking. Often: Repetitive hand motion (such as typing), walking. Seldom: Bending, reaching overhead.
Additional Details Requisition Number:
PRN43957B
Full Time or Part Time?
Full Time
Department:
01167 - HCI Clinical Trials Operations
Location:
Campus
Pay Rate Range:
39300 to 72700
Close Date:
3/31/2026
How to apply To apply, visit
https://utah.peopleadmin.com/postings/194554
Open to qualified applicants. This description is intended to describe the general nature and level of work and is not a comprehensive list of duties and responsibilities.
Posted by the FREE value-added recruitment advertising agency.
Job Function
Information Technology
Industries
Higher Education
Note: This refined description preserves the core content while removing boilerplate, reorganizing into clear sections, and ensuring proper HTML structure with allowed tags.
#J-18808-Ljbffr