Clinical Research Coordinator
5 days ago
Job Summary
As a Clinical Study Coordinator at the University of Nebraska Medical Center, you will play a crucial role in the success of our clinical research activities. We are seeking a highly organized and detail-oriented individual to coordinate diabetes and endocrine studies, recruit patients, and maintain required consents and documentation.
Key Responsibilities
- Coordinate clinical research studies, including recruiting patients and obtaining informed consent
- Maintain accurate and up-to-date records and documentation
- Ensure compliance with study protocols and Institutional Review Board (IRB) regulations
- Provide administrative support to the research team, including data entry and management
- Collaborate with healthcare professionals to ensure smooth study execution
Requirements
- Bachelor's degree in a related field (e.g., healthcare, biology, chemistry)
- 2 years of experience in clinical research or a related field
- Excellent communication and organizational skills
- Ability to work independently and as part of a team
- Attention to detail and ability to maintain confidentiality
Preferred Qualifications
- Phlebotomy certification or willingness to obtain
- Experience with electronic health records and laboratory data management
- Knowledge of study protocols and IRB regulations
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