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Clinical Study Coordinator I

University of Nebraska Medical Center

Location

Omaha, NE, US

Salary

$51,000 - $76,500 /yearly

Type

fulltime

Posted

Today

via indeed

Job Description

Requisition Details

-----------------------

GENERAL REQUISITION INFORMATION

EEO Statement:

UNMC is an Equal Employment Opportunity Employer, including an equal opportunity employer of protected veterans and individuals with disabilities.

Location Omaha, NE

Requisition Number: Staff_14958

Department CHRI Administration 50010500

Business Unit Child Health Research Institute

Reg-Temp Full-Time Regular

Work Schedule Monday - Friday, 8:00AM - 5:00PM

Remote/Telecommuting Hybrid (part-time working on site, part-time working off-site)

Position Summary

Responsible for coordination of patient care during participation in a clinical research trial which includes the complex aspects of health care as it relates to pediatrics and pediatric sub-specialties.

The coordinator assumes responsibility for critical coordination and management of the complex decisions and regulatory requirements of each research protocol.

The coordinator is involved in all aspects of each research protocol facilitating the mission of UNMC and CHRI investigators to effectively participate in clinical research and investigational protocols for a variety of Pediatric specialties.

Position Details

Additional Information

Posting Category Healthcare

Working Title Clinical Study Coordinator I

Job Title Health Care Specialist

Salary Grade HC22S

Appointment Type B1 - REG MGR PROF SALARY

Salary Range $51,000 - $76,500/annual

Job Requisition Begin Date 08/28/2026

Application Review Date 09/04/2026

Review Date Information:

Initial application review will begin on the date provided in the field above. Applications received prior to this review date will be considered. Applications received after the review date may be considered.

Required and Preferred Qualifications

Required Education: Bachelor's degree or equivalent

If any degree major/training is required, please specify the type. (NOTE: Concentration and minors are not equivalent to a major)

(Will consider five years education and/or related experience combined of which two years must include post high school education.)

Required Experience 1 year

If any experience is required, please specify what kind of experience:

Clinical experience and/or research experience in a clinical or laboratory setting

(Will consider five years education and/or related experience combined of which two years must include post high school education)

Required License No

If yes, what is the required licensure/certification?

Required Computer Applications: Microsoft Excel, Microsoft Word

Required Other Computer Applications:

Required Additional Knowledge, Skills and Abilities:

Flexibility in work hours to manage the patient and study protocol workload

Flexibility in work hours to manage the patient and study protocol workload

Reliable and effective verbal and written communication skills

Ability to prioritize and make independent judgments

Possess skills of good organization, flexibility, accountability, being a team player, and self-initiative

Ability to work effectively and collaborate with the interdisciplinary team

Demonstrate knowledge and skill in addressing age specific needs of patients served, (all age groups-birth and above)

Assure performance of behaviors that meet the requirements of the UNMC culture including: demonstrates behavior that fosters a positive team environment, demonstrates behaviors that promote diversity, applies continuous quality improvement principles, seeks the customers requirements and strives to meet them, and designs personal action plan for personal and professional development.

Maintains accountability for own actions in completing assigned tasks.

Preferred Education: Relevant coursework/specialized training or equivalent

If any degree/training is preferred, please specify the type:

Training related to healthcare, laboratory and/or clinical research

Preferred Experience:

Patient-facing clinical research experience, to include clinical trial coordination.

Preferred License: Yes

If yes, what is the preferred licensure/certification?:

Certification/maintenance of certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP)

Preferred Computer Applications: Microsoft Outlook

Preferred Other Computer Applications: Research EDC (i.e. REDcap), EPIC/Electronic Health Records System

Preferred Additional Knowledge, Skills and Abilities:

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