Clinical Research Coordinator II
Full Job Posting
Responsibilities:
- Meets with study participants. Follows study protocol performing duties/testing/data collection. Conducts study required tests and procedures. (Test may include bone density scans, EKG's, balance testing, mental and physical assessments, blood draws, vitals, diary instruction and review, etc.)
- Records data into patient research case report forms (CRF's) to include recording test results and reacting appropriately to abnormal results. Maintains accurate CRF's and source documents
- Schedules appointments for various procedures inside and outside the department. Obtains medical records for any research hospitalizations and various other duties assigned.
- Maintains study drug and supply inventory as well as study drug disbursement
- Reports regulatory and Institutional Review Board issues appropriately (i.e. report adverse events and other regulatory data)
Qualifications:
- Bachelor's Degree in related field (science preferred)
- 4 years clinical experience, preferably in a research setting
- Knowledge of FDA regulatory requirements is required
- Knowledge of the principles of research design
- Ability to maintain confidentiality
- Ability to operate personal computer and various software packages
Preferred Qualifications
- Bachelor's Degree in related field (science preferred)
About Creighton University
Private Jesuit Catholic nonprofit university serving undergraduate, graduate and professional students across health, law, business and arts.
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