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Clinical Study Coordinator

Job in Omaha, Douglas County, Nebraska, 68197, USA
Listing for: University Of Nebraska Medical Center
Part Time position
Listed on 2026-03-01
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Study Coordinator I

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

Location

Omaha, NE

Requisition Number

Department

CHRI Administration

Business Unit

Child Health Research Institute

Reg-Temp

Full-Time Regular

Work Schedule

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

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.

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:

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

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

Required Computer Applications:

Microsoft Excel, Microsoft Word

Required Other Computer Applications:

Required Additional

Knowledge, Skills and Abilities:

  • Knowledge of current nursing procedures, techniques and practices. Ability to perform physical assessments and patient teaching as appropriate to research protocol.
  • Knowledge of performing patient chart reviews.
  • 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 clinical 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:

None Preferred

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

Preferred Experience:

Pediatric background and experience related to clinical trials coordination.

Preferred License:

Yes

Preferred license 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:

Experience with EPIC, REDcap and other research EDC preferred.

Preferred Additional

Knowledge, Skills and Abilities:

  • This position is key to the successful supervision of clinical research trials through monitoring patient care and treatment, protocol regulations, and providing education for patient, family and health care team.
  • Clinical research is based on the collection of information, requiring expert interpretation. Information must be accurately interpreted and recorded to ensure…
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