Clinical research associate [h1.location_city]
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Clinical research associate • omaha ne
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Clinical Research Coordinator
Creighton UniversityOmaha, NE, United States[job_card.variable_days_ago]
[job_preview.job_type]
- [job_card.full_time]
[job_card.job_description]Bachelor's Degree, in a related field of science (preferred). 4 years of clinical experience, ideally within a research setting. Demonstrated understanding of FDA regulatory requirements and clinical research design principles. Basic Life Support (BLS) certification preferred. Attention to detail and commitment to data accuracy. Proficiency in computer systems. Ability to maintain confidentiality and interact effectively with participants and multidisciplinary research teams.
Creighton University is seeking to hire a Clinical Research Coordinator.
Support our clinical research program in the School of Medicine. Under general supervision, this role independently gathers research information, manages the clinical course of research participants according to study protocols, and ensures all activities meet regulatory and ethical standards. This is an hourly paid position.
Schedule : Full-Time | Monday-Friday (occasional evening or weekend hours may be required based on study needs)
Location : CHI Health Creighton University Medical Center- Bergan Mercy (72nd and Mercy Rd). Schedule : Full-Time | Monday-Friday (occasional evening or weekend hours may be required based on study needs)
Key Responsibilities
- Meet with study participants and follow study protocols, performing required duties, tests, and data collection.
- Conduct study-related procedures, which may include bone density scans, EKGs, balance testing, mental and physical assessments, blood draws, vital signs, and diary instruction / review.
- Record data accurately in case report forms (CRFs) and respond appropriately to abnormal test results.
- Schedule participant appointments and coordinate procedures within and outside the department.
- Obtain and review medical records for research-related hospitalizations and maintain organized study documentation.
- Manage study drug inventory and oversee drug disbursement in compliance with research protocols (if applicable).
- Report regulatory and Institutional Review Board (IRB) issues promptly, including adverse events and safety data.
Qualifications