Pediatric Research Nurse Coordinator I

University Of Nebraska Medical Center; Omaha, Northern (NE, KY); Hybrid; USD 65,000 - 90,000; Full time

Job summary

University of Nebraska Medical Center seeks a Clinical Research Nurse Coordinator to oversee patient care and treatment during pediatric trials. You will handle regulatory considerations and coordinate with investigators to ensure protocol fidelity.

Responsibilities include data review, patient education, and collaboration with a multidisciplinary team. Nebraska RN license required, 1 year nursing experience; hybrid schedule with on-site and off-site work.

Qualifications

• Required Education: Nursing (RN)
• Preferred Education: Master’s degree or equivalent
• Required Experience: 1 year in a clinical setting
• Current Nebraska RN license or license eligible
• Proficiency with Excel and Word; Outlook is preferred

Responsibilities

• Coordinate patient care and treatment in clinical research trials.
• Manage regulatory requirements and protocol adherence.
• Train, monitor, and collaborate with pediatric research staff.
• Communicate effectively with physicians, patients, and families.

Education

Nursing (RN)

Master's degree or equivalent

Tools

Microsoft Excel

Microsoft Word

Microsoft Outlook

Research EDC

Job description

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_14317

Department

CHRI Administration 50010500

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 and treatment during participation in a clinical research trial which includes the complex aspects of health care as it relates to pediatrics and pediatric subspecialties. 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: Relevant coursework/specialized training

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

Nursing

Required Experience: 1 year

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

Prior nursing experience in a patient facility or clinical setting.

Required License: No

Current Nebraska RN license or license eligible.

Required Computer Applications: Microsoft Excel, Microsoft Word

• Knowledge of current nursing procedures, techniques and practices
• Ability to perform physical assessments and patient teaching as appropriate to research protocol
• Advanced knowledge of clinical trials and chart review
• Flexibility in work hours to manage the patient and study protocol workload Reliable and effective verbal and written communication skills
• Ability to train, evaluate, and monitor other clinical research staff within the Pediatric Research Office.
• 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: Master's degree or equivalent

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

Preferred Experience:

Pediatric background and experience related to clinical trials coordination.

Preferred License: No

Preferred Computer Applications: Microsoft Outlook

Preferred Other Computer Applications: Research EDC

• Knowledge of healthcare financial environment and reimbursement systems.
• The coordinator is directly responsible to the physician as a physician extender from initial patient contact through follow-up care. The coordinator assumes responsibility for complex decisions that impact the patient care, management, and implementation of specific actions related to clinical research trials. 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 that research results are free of errors. Errors in the interpretation and recording of data may significantly alter research results. Therefore, data entry must be accurate and precise to positively impact patient care and research conclusions.
• Clinical research is based on the collection of information, requiring expert interpretation. Information must be accurately interpreted and recorded to ensure that research results are free of errors. Errors in the interpretation and recording of data may significantly alter research results. Therefore, data entry must be accurate and precise to positively impact patient care and research conclusions.

Required fields are indicated with an asterisk (*).