Job Summary
The Clinical Research Associate I plays a critical role in supporting clinical trials, ensuring compliance with regulatory standards and protocols. This entry-level position is essential for the management and oversight of clinical study activities, providing a foundational understanding of clinical research operations.
Responsibilities
- Assist in the preparation and review of study protocols and documents.
- Monitor clinical trial sites to ensure adherence to study protocols and regulatory requirements.
- Collect and manage study data, ensuring accuracy and integrity.
- Engage in communication with study sites, addressing queries and providing support.
- Participate in the training of site personnel regarding the study protocols.
- Prepare reports and documentation related to site visits and study progress.
Qualifications
- Bachelor’s degree in Life Sciences or a related field.
- Knowledge of clinical research concepts and terminology.
- Strong organizational and communication skills.
- Ability to work in a team environment while managing multiple tasks.
- Attention to detail and commitment to quality in research activities.
University of Nebraska Medical Center provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
