Job Summary
The Clinical Research Coordinator I is responsible for managing the processes of participant screening, enrollment, and retention in clinical studies, while ensuring the collection of high-quality data. This role also involves handling various administrative tasks, including documentation and IRB submissions, and requires collaboration with researchers to conduct intricate laboratory tests and analyze clinical data.
Responsibilities
- Oversee the screening and enrollment processes for study participants.
- Ensure the retention of participants throughout the study.
- Collect and maintain high-quality data for the clinical research projects.
- Handle administrative documentation and submissions to the Institutional Review Board (IRB).
- Collaborate with research teams to perform complex laboratory assays.
- Conduct analysis of clinical data to support research findings.
Qualifications
- Bachelor’s degree in a relevant field, or an equivalent combination of education and experience.
- 1 to 3 years of experience in clinical research is preferred.
- Proficient understanding of Good Clinical Practice (GCP) guidelines.
- Familiarity with clinical data management systems.
University of South Florida 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.
