Job Summary
The Clinical Research Coordinator II is responsible for overseeing research project databases while ensuring adherence to protocols and managing administrative tasks related to clinical trials. This role requires effective interaction with research participants, support in recruitment initiatives, and oversight of specimen collection and processing.
Responsibilities
- Manage and maintain the integrity of research project databases.
- Ensure compliance with clinical trial protocols.
- Perform administrative duties associated with clinical research.
- Engage with research participants and assist in recruitment efforts.
- Supervise the collection and processing of study specimens.
Qualifications
- A minimum of a High School Diploma or GED with five years of clinical research experience.
- A relevant Bachelor’s degree accompanied by one year of clinical research experience.
- Other combinations of education and clinical research experience may be considered based on established minimum qualifications.
Emory University 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.
