Proven experience as a Clinical Research Coordinator or Clinical Research Experience.
At least 1+ year of experience in patient recruitment for clinical research or clinical trials.
Clinical research experience, including familiarity with clinical trial processes and protocols.
Training in HIPAA regulations and patient privacy requirements.
Training in Good Clinical Practice (GCP).
Strong organizational skills with the ability to manage multiple tasks and deadlines.
Confident verbal and written communication skills for interacting with participants, providers, and research staff.
Ability to work effectively in a fast-paced environment while maintaining accuracy and attention to detail.
This is a Contract position based out of Chattanooga, TN.