Clinical Research Coordinator

As the Clinical Research Coordinator, you are responsible for overall clinical operations of the facility’s research program including enrollment, regulatory, quality, and site operations.

• overall clinical operations of the facility’s research program including enrollment, regulatory, quality, and site operations.
• enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements.

• Knowledge of medical and research terminology
• Knowledge of FDA Code of Federal Regulations and GCP
• Knowledge of the clinical research processes

• 401k matching
• Health insurance
• Flight privileges

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials.