clinical study coordinator i - Omaha, NE, United States - University of Nebraska Medical Center
Description
Requisition DetailsGENERAL REQUISITION INFORMATION
EEO Statement:
UNMC is an Affirmative Action Equal Employment Opportunity Employer, including an equal opportunity employer of protected veterans and individuals with disabilities.
Location Omaha, NE Requisition Number:
Staff_12520 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.
Additional Information
Posting Category Healthcare Working Title Clinical Study Coordinator I Job Title Health Care Specialist Salary Grade HC22S Appointment Type B- REG MGR PROF SALARY Salary Range $45,800 - $68,700/annual Job Requisition Begin Date 11/29/2023 Application Review Date 04/21/2024 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 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:
Patient Care Computer Systems, Email and Internet programs, Electronic Data Captures Systems 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.
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 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 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 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.
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