Coordinator - Clinical Research

Catholic Health Initiatives Omaha , NE 68102

Posted 2 months ago

CHI Creighton University Medical Center-Bergan

Your time at work should be fulfilling. Rewarding. Inspiring. That's what you'll find when you join one of our non-profit CHI facilities across the nation. You'll find challenging, rewarding work every day alongside people who have as much compassion as you. Join us and together we'll create healthier, stronger communities. Imagine your career at Catholic Health Initiatives!

Job Summary/Essential Duties:

Recruits, screens, enrolls and obtains consent from program participants.
2.Promotes use of open and available clinical studies to appropriate health care providers and

venues.
3.Conducts and/or coordinates training for program participants.
4.Assures compliance with all relevant IRB and other regulatory agency requirements
5.Serves as subject matter expert for all phases of the research trials as assigned.
6.Collects, manages and maintains patient and laboratory data for clinical research studies
7.Analyzes and abstracts data from departmental and medical record charts to complete and

submit case report forms
8.Maintains and tracks computerized database registration of required research subject data,

including demographics, clinical, laboratory and tracking data

Qualifications

Experience

  • Minimum two years of health care experience in ambulatory or acute care setting, Clinical

Research experience preferred. .

  • Currently holds a Nebraska Medication Aide Registration if not a licensed medical provider or

willing to acquire within one month of employment.

  • Demonstrated knowledge of the clinical trial process and the Federal regulations that govern

the conduct of clinical trials preferred.

Education/Licensure

  • Licensure in Nursing or Pharmacy; BSN, RN,LPN or PharmD; or Certified MA, EMT or Paramedic;

BA, B.S in Health related field required, Combination of course work and/ or relevant

experience in anatomy, physiology, medical terminology, medical records, and information

management, or an equivalent combination of related education and work experience will be

considered.

  • ACRP , SOCRA or other Certification as a Clinical Research Coordinator: CCRC or CCRP

preferred.

  • Valid driver's license
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Coordinator - Clinical Research

Catholic Health Initiatives