Job Summary
The Clinical Research Associate is responsible for overseeing clinical trial operations, which encompass various activities such as screening potential participants, managing their enrollment, and collecting data. This role is crucial in ensuring that all activities comply with regulatory standards, and it also involves maintaining comprehensive study documentation and preparing Institutional Review Board (IRB) applications.
Responsibilities
- Manage participant screening and enrollment processes for clinical trials.
- Oversee data collection and ensure accuracy and completeness.
- Ensure that all clinical trial activities are compliant with regulatory requirements.
- Maintain all study-related documentation and files in an organized manner.
- Prepare and submit applications to the Institutional Review Board (IRB).
Qualifications
- Bachelor’s degree in a relevant field with at least one year of professional experience, or a Master’s degree.
- Must be eligible to work in the United States.
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.
