Clinical Research Coordinator

The Clinical Research Coordinator for Blood Cancer and Bone Marrow Transplant research is responsible for overall clinical operations of the facility’s blood cancer research program including enrollment, regulatory, quality, and site operations.

• Enroll patients onto clinical trials
• Review study design and inclusion/exclusion criteria
• Ensure the protection of study patients
• Collect and enter data into study-specific case report forms
• Coordinate regular site research meetings
• Attend study-specific on-site meetings/visits

• Knowledge of medical and research terminology
• Knowledge of FDA Code of Federal Regulations and GCP
• Knowledge of clinical research processes
• Public presentation skills

• 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.